Prodrugs of a cdk inhibitor for treating cancers

ABSTRACT

There are provided compounds of Formula I, and pharmaceutically acceptable salts and esters thereof, and pharmaceutical compositions thereof, used for inhibition or modulation of the activity of cyclin dependent kinases (CDK) and/or glycogen synthase kinase-3 (GSK-3), for the treatment of disease states or conditions mediated by cyclin dependent kinases and/or glycogen synthase kinase-3, including cancers.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority to Chinese applicationno. 201910343182.5 filed Apr. 26, 2019, the entire contents of which arehereby incorporated by reference.

FIELD

The present disclosure relates to derivatives and prodrugs of4-(2,6-dichlorobenzamido)-N-(4-piperidinyl)-1H-pyrazole-3-carboxamideand compositions thereof that inhibit or modulate the activity of cyclindependent kinases (CDK) and/or glycogen synthase kinase-3 (GSK-3), andtreat disease states or conditions mediated by cyclin dependent kinasesand/or glycogen synthase kinase-3, such as cancers.

BACKGROUND

4-(2,6-Dichlorobenzamido)-N-(4-piperidinyl)-1H-pyrazole-3-carboxamide (apyrazole derivative, also named as4-[(2,6-dichlorobenzoyl)amino]-N-4-piperidinyl-1H-pyrazole-3-carboxamide,4-(2,6-Dichlorobenzoylamino)-1H-pyrazole-3-carboxylic acidN-(piperidin-4-yl)amide, AT7519, AT-7519, or AT7519M) was reported asearly as year 2006 by Berdini and co-workers (see, for example,WO2005012256), with the following chemical structure:

AT7519 is an orally bioavailable small molecule with potentialantineoplastic activity. It selectively binds to and inhibits cyclindependent kinases (CDKs), which may result in cell cycle arrest,induction of apoptosis, and inhibition of tumor cell proliferation. CDKsare serine/theronine kinases involved in regulation of the cell cycleand may be overexpressed in some types of cancer cells. To date, thecompound has appeared in over 100 publications, including patents/patentapplications, and scientific journal papers and communications. Examplesof patents and early patent applications include WO 2006077425, WO2006077416, WO 2006077419, U.S. Pat. No. 7,385,059, and US2010021420.Examples of scientific papers include “Identification ofN-(4-Piperidinyl)-4-(2,6-dichlorobenzoylamino)-1H-pyrazole-3-carboxamide(AT7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment-BasedX-Ray Crystallography and Structure Based Drug Design” (Wyatt, et al.,J. Med. Chem., 2008, 51(16), 4986-4999), “Biological characterization ofAT7519, a small-molecule inhibitor of cyclin-dependent kinases, in humantumor cell lines” (Squires, et al., Mol. Cancer Ther., 2009, 8(2),324-332), “AT7519, a Cyclin-Dependent Kinase Inhibitor, Exerts ItsEffects by Transcriptional Inhibition in Leukemia Cell Lines and PatientSamples” (Squires, et al., Mol. Cancer Ther., 2010, 9(4), 920-928), and“AT7519, A novel small molecule multi-cyclin-dependent kinase inhibitor,induces apoptosis in multiple myeloma via GSK-3β activation and RNApolymerase II inhibition” (Santo, et al., Oncogene, 2010, 29(16),2325-2336).

Many studies have demonstrated potential therapeutic use of AT7519 intreating cancers. AT7519 is an ATP competitive CDK inhibitor with aK_(i) value of 38 nM for CDK1. AT7519 is inactive against all non-CDKkinases with the exception of GSK3β (IC50=89 nM). AT7519 shows potentantiproliferative activity in a variety of human tumor cell lines withIC50 values ranging from 40 nM for MCF-7 to 940 nM for SW620 consistentwith the inhibition of CDK1 and CDK2 (Squires M S, et al. Mol. CancerTher, 2009, 8(2), 324-332). AT7519 induces dose-dependent cytotoxicityin multiple myeloma (MM) cell lines with IC50 values ranging from 0.5 to2 μM at 48 hours, with the most sensitive cell lines being MM.1S (0.5μM) and U266 (0.5 μM) and the most resistant MM.1R (>2 μM). It does notinduce cytotoxicity in peripheral blood mononuclear cells (PBMNC).AT7519 partially overcomes the proliferative advantage conferred by IL6and IGF-1 as well as the protective effect of bone marrow stromal cells(BMSCs). AT7519 induces rapid dephosphorylation of RNA pol II CTD atserine 2 and serine 5 sites, and leads to the inhibition oftranscription, partially contributing to AT7519 induced cytotoxicity ofMM cells. AT7519 also induces activation of GSK-3β by down-regulatingGSK-3β phosphorylation, which may contribute to AT7519 induced apoptosisindependent of the inhibition of transcription (Santo L, et al.Oncogene, 2010, 29(16), 2325-2336).

A twice daily dosing of AT7519 (9.1 mg/kg) has been shown to cause tumorregression of both early-stage and advanced-stage s.c. tumors in theHCT116 and HT29 colon cancer xenograft models (Squires MS, et al. Mol.Cancer Ther, 2009, 8(2), 324-332). AT7519 treatment (15 mg/kg) caninhibit tumor growth and prolong the median overall survival of mice inthe human MM xenograft mouse model in association with increased caspase3 activation (Santo L, et al. Oncogene, 2010, 29(16), 2325-2336).

AT7519 has been considered a potential therapeutic for a variety ofindications including multiple myeloma, mantle cell lymphoma, chroniclymphocytic leukemia, solid tumor, non-Hodgkin lymphoma, andhematological neoplasm. Several clinical trials to test AT-7519 in thetreatment of multiple myeloma (MM), chronic lymphocytic leukemia (CLL),and solid tumors including mantle cell lymphoma (MCL) have also beeninitiated (see for example, “A Phase I study of cyclin-dependent kinaseinhibitor, AT7519, in patients with advanced cancer: NCIC ClinicalTrials Group IND 177” (Chen, E. X., et al., Br. J. of Cancer, 2014,111(12), 2262-2267)). However, because of the involvement of AT7519 inmultiple pathways essential for transcription and proliferation, thepotential for adverse events is high. Indeed, AT7519 has shown asignificant level of toxicity in both animal and human testing. Themajority of patients treated with AT7519 had at least onetreatment-related AE (82.1%). The majority of AEs were CommonTerminology Criteria for Adverse Events grade 1 or 2 in severity (46.7%and 37.8%, respectively). The most common treatment-emergent AEs werenausea (50.0%), fatigue (42.9%), vomiting and anorexia (39.3% each),constipation (32.1%) and peripheral edema, pyrexia and hypotension(25.0% each) (Mahadevan, D; et al., Ann. Oncol., 2011, 22:2137-2143). Ina phase I clinical trial, AT7519M dose was escalated to 32.4 mg/m².Among the initial three patients enrolled, one patient experienced DLT(grade 3 fatigue). Two additional patients were enrolled at this doselevel, both of whom experienced DLTs (febrile neutropenia and grade 3hypokalemia and mucositis) (Chen, E. X.; et al., Br. J. Cancer, 2014,111:2262-2267).

It would be desirable to enhance potency and/or reduce toxicity ofAT7519 for therapeutic use.

SUMMARY

It is an object of the present invention to ameliorate at least some ofthe deficiencies present in the prior art. Embodiments of the presenttechnology have been developed based at least in part on the inventors'appreciation that there is a need for reducing the toxicity of4-(2,6-dichlorobenzamido)-N-(4-piperidinyl)-1H-pyrazole-3-carboxamide(AT7519) for its use in therapeutic applications. These and other needscan be satisfied by the disclosure herein of AT7519 derivatives and/orprodrugs, pharmaceutical compositions and uses thereof to inhibit ormodulate the activity of a cyclin dependent kinase (CDK) and/or glycogensynthase kinase-3 (GSK-3), and treat disease states or conditionsmediated by cyclin dependent kinases and/or glycogen synthase kinase-3,such as cancers.

In a first aspect, there are provided compounds of Formula I, orpharmaceutically acceptable salts or esters thereof:

where R¹ and R² are independently a hydrogen (H) or a protecting group(P), and the protecting groups are the same or different, provided atleast one of R¹ and R² is not a hydrogen.

In one embodiment R¹ and R² are both independently a protecting groupselected from: acyl, carbonyl, thiocarbonyl, and carbamoyl groups;substituted or unsubstituted acetyl, aminoalkanoyl, and α-aminoalkanoyl;substituted or unsubstituted acyl groups derived from a natural orunnatural amino acid; substituted or unsubstituted acyl groups ofpeptide residues; substituted or unsubstituted cycloalkane-carbonyl,heterocycloalkane-carbonyl, alkoxycarbonyl, aryloxycarbonyl,heteroalkoxycarbonyl, or heteroaryloxycarbonyl; and O-substitutedhydroxymethyl group. In an embodiment, R¹ and R² are the same protectinggroup. In another embodiment, R¹ and R² are different protecting groups.

In another embodiment, R¹ and R² are independently a hydrogen or aprotecting group having the structure R³W(R⁴R⁵C)_(m)—, where: m is aninteger selected from 1 to 6; W is oxygen (—O—), sulfur (—S—), nitrogen(—NH—), or absent; R⁴ and R⁵ are independently hydrogen or lower alkylgroup; and R³ is

where:

X is oxygen (—O—), sulfur (—S—), nitrogen (—NH—), or a methylene (—CH₂—)group;

R⁶ and R⁷ are independently a hydrogen; a substituted or unsubstitutedalkyl or cycloalkyl; an aryl or heteroaryl group without or withsubstitution; a PEG moiety having the structure R⁸—(OCH₂CH₂)_(n)—, wheren=1 to 10, and R⁸ is a hydrogen or a lower alkyl; an ester-forming groupsuch as a lower alkyl or an aryl group; or a salt-forming moiety when Xis oxygen or sulfur, such as a sodium, a potassium, atetraethylammonium, or a tetrabutylammonium; or the combination of R⁶and X is an alky or aryl group with or without further substitution;provided at least one of R¹ and R² is not a hydrogen.

In a further embodiment, R² is a hydrogen, R¹ is a protecting groupselected from acyl, carbonyl, thiocarbonyl, and carbamoyl groups;substituted or unsubstituted acetyl, aminoalkanoyl, and α-aminoalkanoyl;acyl groups derived from a natural or unnatural amino acid with orwithout substitution; acyl groups of peptide residues; substituted orunsubstituted cycloalkane-carbonyl, heterocycloalkane-carbonyl,alkoxycarbonyl, aryloxycarbonyl, heteroalkoxycarbonyl, orheteroaryloxycarbonyl; O-substituted hydroxymethyl group with or withoutsubstituents; and R³W(R⁴R⁵C)_(m)—, where m=0 to 6 and W, X, R³, R⁴, andR⁵ are as defined above.

In another embodiment, R¹ is a hydrogen, and R² is R³W(R⁴R⁵C)_(m)—,where m is an integer selected from 1 to 6, and W, X, R³, R⁴, and R⁵ areas defined above.

In a further embodiment, R¹ and R² are independently selected from ahydrogen,

where X, R⁶ and R⁷ are as defined above and R⁹ is a substituent group,provided that one of R¹ and R² is not a hydrogen. In some embodiments,R⁹ is a substituent group selected from lower alkyl, hydroxyl, halogen(—F, —Cl, —Br, or —I), nitro, amino, lower alkyl amino, and loweralkyloxy group.

In some embodiments, the compound of Formula I is a compound shown inTable 1, or a pharmaceutically-acceptable salt, ester, chelate, hydrate,solvate, stereoisomer, or polymorphic form thereof.

In some embodiments, the compound of Formula I is a derivative or aprodrug of AT7519.

TABLE 1 Examples of compounds of Formula I. No. Structure  1

 2

 3

 4

 5

 6

 7

 8

 9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

25

26

27

28

29

30

31

32

33

34

35

36

37

38

39

40

41

42

43

44

45

46

47

48

49

50

51

52

53

54

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56

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58

59

60

61

62

63

64

65

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71

72

73

74

In some embodiments, compounds provided herein are inhibitors of cyclindependent kinases, and in particular cyclin dependent kinases selectedfrom CDK1, CDK2, CDK3, CDK4, CDK5, CDK6, CDK7 and CDK9. In someembodiments, compounds can inhibit one or more CDK kinase selected fromCDK1, CDK2, CDK4, CDK5, CDK6, and CDK9. In an embodiment, the compoundinhibits CDK1, CDK2, or both CDK1 and CDK2. In an embodiment, thecompound inhibits CDK4, CDK6, or both CDK4 and CDK6. In embodiments,compounds provided herein are, additionally or alternatively, inhibitorsof glycogen synthase kinase-3 (GSK3).

In some embodiments, compounds provided herein are prodrugs of AT7519.

In a second broad aspect, there are provided pharmaceutical compositionscomprising a compound described herein, or a pharmaceutically acceptablesalt or ester thereof, and a pharmaceutically acceptable carrier. Insome embodiments, there are provided pharmaceutical compositionscomprising a compound of Formula I, or a pharmaceutically acceptablesalt or ester thereof, and a pharmaceutically acceptable carrier.

In a third broad aspect, there are provided methods of inhibiting ormodulating the activity of a cyclin dependent kinase (CDK) and/orglycogen synthase kinase-3 (GSK-3). In some embodiments, there areprovided methods of treating disease states or conditions mediated bycyclin dependent kinases and/or glycogen synthase kinase-3 in a subjectin need thereof comprising administering to the subject an effectiveamount of a compound and/or a pharmaceutical composition describedherein. Non-limiting examples of disease states or conditions mediatedby cyclin dependent kinases and/or glycogen synthase kinase-3 that maybe treated according to methods provided herein include viralinfections, type II or non-insulin dependent diabetes mellitus,autoimmune diseases, head trauma, stroke, epilepsy, neurodegenerativediseases such as Alzheimer's, motor neuron disease, progressivesupranuclear palsy, corticobasal degeneration and Pick's disease, anddisorders of proliferation, apoptosis or differentiation, such asvarious tumors and cancers. In particular embodiments, compounds areuseful for treatment of viral infections, autoimmune diseases and/orneurodegenerative diseases.

In other embodiments, compounds are useful for treatment of tumors andcancers. Examples of tumors and cancers that may be treated according tomethods provided herein include, without limitation: multiple myeloma(MM), chronic lymphocytic leukemia (CLL), acute myeloid leukemia (AML),mantle cell lymphoma (MCL), solid tumors, refractory solid tumors,non-Hodgkin lymphoma, carcinoma of the colon, hematological neoplasm,and myelodysplastic syndromes (MDS). Other tumors and cancers include,without limitation: neuroblastoma, colorectal cancer, cervical cancer,lung cancer, leukemia, breast cancer, pancreatic cancer, B-cellmalignancies, neoplasms, and metastatic tumors.

In some embodiments, compounds provided herein and/or pharmaceuticalcompositions thereof are administered to reduce the therapeutic toxicityand/or adverse effects, and/or increase tolerability of AT7519, and/orimprove therapeutic effect in a subject, as compared to administrationof AT7519.

In other embodiments, compounds provided herein and/or pharmaceuticalcompositions thereof are administered to improve biodistribution ofAT7519, to reduce the side effects of AT7519, and/or to broaden thetherapeutic application (such as dose regimen, including the routes ofadministration, dose frequency, and maximum tolerated dose, etc.) in asubject, as compared to administration of AT7519 itself.

In another broad aspect, there are provided kits comprising one or morecompound or pharmaceutical composition described herein. A kit mayfurther comprise one or more additional therapeutic agents and/orinstructions, for example, instructions for using the kit to treat asubject having disease states or conditions mediated by cyclin dependentkinases and/or glycogen synthase kinase-3.

BRIEF DESCRIPTION OF THE DRAWINGS

For a better understanding of the invention and to show more clearly howit may be carried into effect, reference will now be made by way ofexample to the accompanying drawings, which illustrate aspects andfeatures according to embodiments of the present invention, and inwhich:

FIG. 1 shows plasma AT7519 concentration-time curves after intravenousadministration of AT7519, compound 11, and compound 12 to mice.

FIG. 2 shows body-weight changes with time after intravenousadministration of AT7519, compound 11, and compound 12 to mice.

FIG. 3 shows plasma AT7519 concentration-time curves after intravenousadministration of AT7519, compound 11, and compound 12 atmolar-equivalent dose to rats.

DETAILED DESCRIPTION Definitions

In order to provide a clear and consistent understanding of the termsused in the present specification, a number of definitions are providedbelow. Moreover, unless defined otherwise, all technical and scientificterms as used herein have the same meaning as commonly understood to oneof ordinary skill in the art to which this invention pertains.

The use of the word “a” or “an” when used in conjunction with the term“comprising” in the claims and/or the specification may mean “one”, butit is also consistent with the meaning of “one or more”, “at least one”,and “one or more than one”. Similarly, the word “another” may mean atleast a second or more.

As used in this specification and claim(s), the words “comprising” (andany form of comprising, such as “comprise” and “comprises”), “having”(and any form of having, such as “have” and “has”), “including” (and anyform of including, such as “include” and “includes”) or “containing”(and any form of containing, such as “contain” and “contains”), areinclusive or open-ended and do not exclude additional, unrecitedelements or process steps.

The term “about” is used to indicate that a value includes an inherentvariation of error for the device or the method being employed todetermine the value.

The term “derivative” as used herein, is understood as being a substancesimilar in structure to another compound but differing in some slightstructural detail.

The present description refers to a number of chemical terms andabbreviations used by those skilled in the art. Nevertheless,definitions of selected terms are provided for clarity and consistency.

As used herein, the term “substituted” or “with substitution” refers toa parent compound or a moiety has at least one (1) substituent group.The term “unsubstituted” or “without substitution” refers to a parentcompound or a moiety has no other substituent group except that theunidentified valence is chemically saturated with hydrogen atoms.

As used herein, a “substituent” or a “substituent group” refers to agroup selected from halogen (F, Cl, Br, or I), hydroxy, sulfhydryl,amino, nitro, carbonyl, carboxyl, alkyl, alkoxyl, alkylamino, aryl,aryloxyl, acylamino, acyl, thionyl, sulfonyl, phosphonyl, or otherorganic moiety as used and accepted in general organic chemistry.

As used herein, the term “alkyl” refers to saturated hydrocarbons havingfrom one to twelve carbon atoms, including linear, branched, and cyclicalkyl groups. Examples of alkyl groups include, without limitation,methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl,decyl, isopropyl, tert-butyl, sec-butyl, isobutyl, cyclopropyl,cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and the like. The termalkyl includes both unsubstituted alkyl groups and substituted alkylgroups. The term “C₁-C_(n)alkyl”, wherein n is an integer from 2 to 12,refers to an alkyl group having from 1 to the indicated “n” number ofcarbon atoms. Alkyl residues may be substituted or unsubstituted. Insome embodiments, for example, alkyl may be substituted by hydroxyl,amino, carboxyl, carboxylic ester, amide, carbamate, or aminoalkyl.

Unless the number of carbons is otherwise specified, “lower” as in“lower aliphatic,” “lower alkyl,” “lower alkenyl,” and “lower alkylnyl”,as used herein means that the moiety has at least one (two for alkenyland alkynyl) and equal to or less than 6 carbon atoms.

The terms “cycloalkyl”, “alicyclic”, “carbocyclic” and equivalentexpressions refer to a group comprising a saturated or partiallyunsaturated carbocyclic ring in a single, spiro (sharing one atom), orfused (sharing at least one bond) carbocyclic ring system having fromthree to fifteen ring members. Examples of cycloalkyl groups include,without limitation, cyclopropyl, cyclobutyl, cyclopentyl,cyclopenten-1-yl, cyclopenten-2-yl, cyclopenten-3-yl, cyclohexyl,cyclohexen-1-yl, cyclohexen-2-yl, cyclohexen-3-yl, cycloheptyl,bicyclo[4,3,0]nonanyl, norbornyl, and the like. The term cycloalkylincludes both unsubstituted cycloalkyl groups and substituted cycloalkylgroups. The term “C₃-C_(n)cycloalkyl”, wherein n is an integer from 4 to15, refers to a cycloalkyl group having from 3 to the indicated “n”number of carbon atoms in the ring structure. Unless the number ofcarbons is otherwise specified, “lower cycloalkyl” groups as hereinused, have at least 3 and equal to or less than 8 carbon atoms in theirring structure.

Cycloalkyl residues can be saturated or contain one or more double bondswithin the ring system. In particular they can be saturated or containone double bond within the ring system. In unsaturated cycloalkylresidues the double bonds can be present in any suitable positions.Monocycloalkyl residues are, for example, cyclopropyl, cyclobutyl,cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl,cycloheptenyl, cyclooctyl, cyclononyl, cyclodecyl, cycloundecyl,cyclododecyl or cyclotetradecyl, which can also be substituted, forexample by C₁₋₄ alkyl. Examples of substituted cycloalkyl residues are4-methylcyclohexyl and 2,3-dimethylcyclopentyl. Examples of parentstructures of bicyclic ring systems are norbornane,bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane and bicyclo[3.2.1]octane.

The term “heterocycloalkyl” and equivalent expressions refer to a groupcomprising a saturated or partially unsaturated carbocyclic ring in asingle, spiro (sharing one atom), or fused (sharing at least one bond)carbocyclic ring system having from three to fifteen ring members,including one to six heteroatoms (e.g., N, O, S, P) or groups containingsuch heteroatoms (e.g., NH, NR_(x) (R_(x) is alkyl, acyl, aryl,heteroaryl or cycloalkyl), PO₂, SO, SO₂, and the like). Heterocycloalkylgroups may be C-attached or heteroatom-attached (e.g., via a nitrogenatom) where such is possible. Examples of heterocycloalkyl groupsinclude, without limitation, pyrrolidino, tetrahydrofuranyl,tetrahydrodithienyl, tetrahydropyranyl, tetrahydrothiopyranyl,piperidino, morpholino, thiomorpholino, thioxanyl, piperazinyl,azetidinyl, oxetanyl, thietanyl, homopiperidinyl, oxepanyl, thiepanyl,oxazepinyl, diazepinyl, thiazepinyl, 1,2,3,6-tetrahydropyridinyl,2-pyrrolinyl, 3-pyrrolinyl, indolinyl, 2H-pyranyl, 4H-pyranyl, dioxanyl,1,3-dioxolanyl, pyrazolinyl, dithianyl, dithiolanyl, dihydropyranyl,dihydrothienyl, dihydrofuranyl, pyrazolidinyl, imidazolinyl,imidazolidinyl, 3-azabicyclo[3,1,0]hexanyl, 3-azabicyclo[4,1,0]heptanyl,3H-indolyl, quinolizinyl, and sugars, and the like. The termheterocycloalkyl includes both unsubstituted heterocycloalkyl groups andsubstituted heterocycloalkyl groups. The term“C₃-C_(n)heterocycloalkyl”, wherein n is an integer from 4 to 15, refersto a heterocycloalkyl group having from 3 to the indicated “n” number ofatoms in the ring structure, including at least one hetero group or atomas defined above. Unless the number of carbons is otherwise specified,“lower heterocycloalkyl” groups as herein used, have at least 3 andequal to or less than 8 carbon atoms in their ring structure.

The terms “aryl” and “aryl ring” refer to aromatic groups having“4n+2”.pi.(pi) electrons, wherein n is an integer from 1 to 3, in aconjugated monocyclic or polycyclic system (fused or not) and having sixto fourteen ring atoms. A polycyclic ring system includes at least onearomatic ring. Aryl may be directly attached, or connected via aC₁-C₃alkyl group (also referred to as arylalkyl or aralkyl). Examples ofaryl groups include, without limitation, phenyl, benzyl, phenetyl,1-phenylethyl, tolyl, naphthyl, biphenyl, terphenyl, indenyl,benzocyclooctenyl, benzocycloheptenyl, azulenyl, acenaphthylenyl,fluorenyl, phenanthernyl, anthracenyl, and the like. The term arylincludes both unsubstituted aryl groups and substituted aryl groups. Theterm “C₆-C_(n)aryl”, wherein n is an integer from 6 to 15, refers to anaryl group having from 6 to the indicated “n” number of atoms in thering structure, including at least one hetero group or atom as definedabove.

The terms “heteroaryl” and “heteroaryl ring” refer to an aromatic groupshaving “4n+2”.pi.(pi) electrons, wherein n is an integer from 1 to 3, ina conjugated monocyclic or polycyclic system (fused or not) and havingfive to fourteen ring members, including one to six heteroatoms (e.g. N,O, S) or groups containing such heteroatoms (e.g. NH, NR_(x) (R_(x) isalkyl, acyl, aryl, heteroaryl or cycloalkyl), SO, and the like). Apolycyclic ring system includes at least one heteroaromatic ring.Heteroaryls may be directly attached, or connected via a C₁-C₃alkylgroup (also referred to as heteroarylalkyl or heteroaralkyl). Heteroarylgroups may be C-attached or heteroatom-attached (e.g., via a nitrogenatom), where such is possible. Examples of heteroaryl groups include,without limitation, pyridyl, imidazolyl, pyrimidinyl, pyrazolyl,triazolyl, tetrazolyl, furyl, thienyl; isooxazolyl, thiazolyl, oxazolyl,isothiazolyl, pyrrollyl, quinolinyl, isoquinolinyl, indolyl, isoindolyl,chromenyl, isochromenyl, benzimidazolyl, benzofuranyl, cinnolinyl,indazolyl, indolizinyl, phthalazinyl, pyridazinyl, pyrazinyl, triazinyl,isoindolyl, pteridinyl, purinyl, oxadiazolyl, thiadiazolyl, furazanyl,benzofurazanyl, benzothiophenyl, benzothienyl, benzothiazolyl,benzoxazolyl, quinazolinyl, quinolizinyl, quinolonyl, isoquinolonyl,quinoxalinyl, naphthyridinyl, furopyridinyl, carbazolyl,phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl,phenothiazinyl, phenoxazinyl, dibenzofurnayl, and the like. The termheteroaryl includes both unsubstituted heteroaryl groups and substitutedheteroaryl groups. The term “C₅-C_(n)heteroaryl”, wherein n is aninteger from 6 to 15, refers to a heteroaryl group having from 5 to theindicated “n” number of atoms in the ring structure, including at leastone hetero group or atom as defined above.

The terms “heterocycle” or “heterocyclic” include heterocycloalkyl andheteroaryl groups. Examples of heterocycles include, without limitation,acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl,benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl,benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl,carbazolyl, 4αH-carbazolyl, carbolinyl, chromanyl, chromenyl,cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl,dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl,imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl,indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl,isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl,isoxazolyl, methylenedioxyphenyl, morpholinyl, naphthyridinyl,octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl,1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl,oxazolyl, oxazolidinyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl,phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl,piperazinyl, piperidinyl, piperidonyl, 4-piperidonyl, piperonyl,pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl,pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole,pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl,pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl,quinuclidinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl,tetrahydroquinolinyl, tetrazolyl, 6H-1,2,5-thiadiazinyl,1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl,1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl,thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl,1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl,xanthenyl, and the like. The term heterocycle includes bothunsubstituted heterocyclic groups and substituted heterocyclic groups.

The term “amine” or “amino,” as used herein, refers to an unsubstitutedor substituted moiety of the formula —NR^(a)R^(b), in which R^(a) andR^(b) are each independently hydrogen, alkyl, aryl, or heterocyclyl, orR^(a) and R^(b), taken together with the nitrogen atom to which they areattached, form a heterocyclic ring. The term amino includes compounds ormoieties in which a nitrogen atom is covalently bonded to at least onecarbon or heteroatom. Thus, the terms “alkylamino” and “dialkylamino” asused herein mean an amine group having respectively one and at least twoC₁-C₆alkyl groups attached thereto. The terms “arylamino” and“diarylamino” include groups wherein the nitrogen is bound to at leastone or two aryl groups, respectively. The terms “amide” or“aminocarbonyl” include compounds or moieties which contain a nitrogenatom which is bound to the carbon of a carbonyl or a thiocarbonyl group.The term “acylamino” refers to an amino group directly attached to anacyl group as defined herein.

The term “alkylthio” refers to an alkyl group, having a sulfhydryl groupattached thereto. Suitable alkylthio groups include groups having 1 toabout 12 carbon atoms, preferably from 1 to about 6 carbon atoms. Theterm “alkylcarboxyl” as used herein means an alkyl group having acarboxyl group attached thereto.

The terms “alkoxy” or “lower alkoxy” as used herein mean an alkyl grouphaving an oxygen atom attached thereto. Representative alkoxy groupsinclude groups having 1 to about 6 carbon atoms, e.g., methoxy, ethoxy,propoxy, tert-butoxy and the like. Examples of alkoxy groups includemethoxy, ethoxy, isopropyloxy, propoxy, butoxy, pentoxy, fluoromethoxy,difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy,trichloromethoxy groups, and the like. The term “alkoxy” includes bothunsubstituted or substituted alkoxy groups, etc., as well asperhalogenated alkyloxy groups.

The terms “carbonyl” or “carboxy” include compounds and moieties whichcontain a carbon connected with a double bond to an oxygen atom.Examples of moieties which contain a carbonyl include aldehydes,ketones, carboxylic acids, amides, esters, anhydrides, etc.

The term “acyl” refers to a carbonyl group that is attached through itscarbon atom to a hydrogen (i.e., formyl), an aliphatic group(C1-C6alkyl, C1-C6alkenyl, C1-C6alkynyl, e.g., acetyl), a cycloalkylgroup (C3-C8cycloalkyl), a heterocyclic group (C3-C8 heterocycloalkyland C5-C6 heteroaryl), an aromatic group (C6 aryl, e.g., benzoyl), andthe like. Acyl groups may be unsubstituted or substituted acyl groups(e.g., salicyloyl).

The term “solvate” refers to a physical association of a compound withone or more solvent molecules, whether organic or inorganic. Thisphysical association includes hydrogen bonding. In certain instances, asolvate will be capable of isolation, for example when one or moresolvent molecules are incorporated in the crystal lattice of acrystalline solid. “Solvate” encompasses both solution-phase andisolable solvates. Exemplary solvates include, without limitation,hydrates, ethanolates, methanolates, hemiethanolates, and the like. Theterm “hydrate” refers to a physical association of a compound with watermolecules.

The term “chelate” refers to a physical association of a compound with acentral metal atom, typically bonded at two or more points, often in acyclic or ring structure.

It should be understood that compounds described herein may contain oneor more chiral centers and/or double bonds and therefore, may exist asstereoisomers, such as double-bond isomers (i.e., geometric isomers),enantiomers, or diastereomers. Chemical structures disclosed herein areintended to encompass all possible enantiomers and stereoisomers of theillustrated compounds including the stereoisomerically pure form (e.g.,geometrically pure, enantiomerically pure, or diastereomerically pure)and enantiomeric and stereoisomeric mixtures. Enantiomeric andstereoisomeric mixtures can be resolved into their component enantiomersor stereoisomers using separation techniques or chiral synthesistechniques well known to the skilled artisan, e.g., chiralchromatography (such as chiral HPLC), immunoassay techniques, or the useof covalently (such as Mosher's esters) and non-covalently (such aschiral salts) bound chiral reagents to respectively form adiastereomeric mixture which can be separated by conventional methods,such as chromatography, distillation, crystallization or sublimation,the chiral salt or ester is then exchanged or cleaved by conventionalmeans, to recover the desired isomers. The compounds may also exist inseveral tautomeric forms including the enol form, the keto form, andmixtures thereof. The chemical structures depicted herein are alsointended to encompass all possible tautomeric forms of the illustratedcompounds.

Certain compounds may exist in multiple crystalline or amorphous forms.In general, all physical forms are intended to be encompassed herein.The term “polymorphic form” refers to the various physical forms that acompound may display.

A “pharmaceutically acceptable salt” of a compound means a salt of acompound that is pharmaceutically acceptable. Desirable are salts of acompound that retain or improve the biological effectiveness andproperties of the free acids and bases of the parent compound as definedherein or that take advantage of an intrinsically basic, acidic orcharged functionality on the molecule and that are not biologically orotherwise undesirable. Examples of pharmaceutically acceptable salts arealso described, for example, in Berge et al., “Pharmaceutical Salts”, J.Pharm. Sci. 66, 1-19 (1977). Non-limiting examples of such saltsinclude:

(1) acid addition salts, formed on a basic or positively chargedfunctionality, by the addition of inorganic acids such as hydrochloricacid, hydrobromic acid, hydroiodic acid, sulfuric acid, sulfamic acid,nitric acid, phosphoric acid, carbonate forming agents, and the like; orformed with organic acids such as acetic acid, propionic acid, lacticacid, oxalic, glycolic acid, pivalic acid, t-butylacetic acid,β-hydroxybutyric acid, valeric acid, hexanoic acid,cyclopentanepropionic acid, pyruvic acid, malonic acid, succinic acid,malic acid, maleic acid, fumaric acid, tartaric acid, citric acid,benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelicacid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonicacid, 2-hydroxyethanesulfonic acid, cyclohexylaminosulfonic acid,benzenesulfonic acid, sulfanilic acid, 4-chlorobenzenesulfonic acid,2-napthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid,3-phenyl propionic acid, lauryl sulphonic acid, lauryl sulfuric acid,oleic acid, palmitic acid, stearic acid, lauric acid, embonic (pamoic)acid, palmoic acid, pantothenic acid, lactobionic acid, alginic acid,galactaric acid, galacturonic acid, gluconic acid, glucoheptonic acid,glutamic acid, naphthoic acid, hydroxynapthoic acid, salicylic acid,ascorbic acid, stearic acid, muconic acid, and the like;

(2) base addition salts, formed when an acidic proton present in theparent compound either is replaced by a metal ion, including, an alkalimetal ion (e.g., lithium, sodium, potassium), an alkaline earth ion(e.g., magnesium, calcium, barium), or other metal ions such asaluminum, zinc, iron and the like; or coordinates with an organic basesuch as ammonia, ethylamine, diethylamine, ethylenediamine,N,N′-dibenzylethylenediamine, ethanolamine, diethanolamine,triethanolamine, tromethamine, N-methylglucamine, piperazine,chloroprocain, procain, choline, lysine and the like.

Pharmaceutically acceptable salts may be synthesized from a parentcompound that contains a basic or acidic moiety, by conventionalchemical methods. Generally, such salts are prepared by reacting thefree acid or base forms of compounds with a stoichiometric amount of theappropriate base or acid in water or in an organic solvent, or in amixture of the two. Salts may be prepared in situ, during the finalisolation or purification of a compound or by separately reacting acompound in its free acid or base form with the desired correspondingbase or acid, and isolating the salt thus formed. The term“pharmaceutically acceptable salts” also include zwitterionic compoundscontaining a cationic group covalently bonded to an anionic group, asthey are “internal salts”. It should be understood that all acid, salt,base, and other ionic and non-ionic forms of compounds described hereinare intended to be encompassed. For example, if a compound is shown asan acid herein, the salt forms of the compound are also encompassed.Likewise, if a compound is shown as a salt, the acid and/or basic formsare also encompassed.

As used herein the term “effective amount” refers to the amount or doseof a therapeutic agent, such as a compound, upon single or multiple doseadministration to a subject, which provides the desired therapeutic,diagnostic, or prognostic effect in the subject. An effective amount canbe readily determined by an attending physician or diagnostician usingknown techniques and by observing results obtained under analogouscircumstances. In determining the effective amount or dose of compoundadministered, a number of factors are considered including, but notlimited to: the size, age, and general health of the subject; thespecific disease involved; the degree of or involvement or the severityof the disease or condition to be treated; the response of theindividual subject; the particular compound administered; the mode ofadministration; the bioavailability characteristics of the preparationadministered; the dose regimen selected; the use of concomitantmedication(s); and other relevant considerations.

“Pharmaceutically acceptable” refers to drugs, medicaments, inertingredients etc., which the term describes, suitable for use in contactwith the cells or tissues of humans and animals without undue toxicity,incompatibility, instability, irritation, allergic response, and thelike, commensurate with a reasonable benefit/risk ratio. It generallyrefers to a compound or composition that is approved or approvable by aregulatory agency of the Federal or state government or listed in theU.S. Pharmacopoeia or other generally recognized pharmacopoeia for usein animals and more particularly in humans.

“Pharmaceutically acceptable vehicle” refers to a diluent, adjuvant,excipient, vehicle or carrier with which a compound is administered. Theterms “Pharmaceutically acceptable vehicle” and “Pharmaceuticallyacceptable carrier” are used interchangeably herein.

“Pharmaceutical composition” refers to a composition comprising acompound as described herein and at least one component comprising apharmaceutically acceptable carrier, diluent, adjuvant, excipient, orvehicle, such as a preserving agent, a filler, a disintegrating agent, awetting agent, an emulsifying agent, a suspending agent, a sweeteningagent, a flavoring agent, a perfuming agent, an antibacterial agent, anantifungal agent, a lubricating agent, a dispensing agent, and the like,depending on the nature of the mode of administration and dosage forms.

“Preventing” or “prevention” is intended to refer to at least thereduction of likelihood of the risk of (or susceptibility to) acquiringa disease or disorder (i.e., causing at least one of the clinicalsymptoms of the disease not to develop in a patient that may be exposedto or predisposed to the disease but does not yet experience or displaysymptoms of the disease).

“Treating” or “treatment” of any disease or disorder refers, in someembodiments, to ameliorating at least one disease or disorder. Incertain embodiments “treating” or “treatment” refers to ameliorating atleast one physical parameter, which may or may not be discernible by thepatient. In certain embodiments, “treating” or “treatment” refers toinhibiting the disease or disorder, either physically, (e.g.,stabilization of a discernible symptom), physiologically, (e.g.,stabilization of a physical parameter), or both. In some embodiments,“treating” or “treatment” refers to improving the quality of life orreducing the symptoms or side effects of a disease in a subject in needthereof “Therapeutically effective amount” means the amount of acompound that, when administered to a subject for treating or preventinga disease, is sufficient to effect such treatment or prevention of thedisease. The “therapeutically effective amount” will vary depending onthe compound, the disease and its severity, and the age, weight, etc.,of the subject having the disease to be treated or prevented. As usedherein, the term “therapeutically effective amount” refers to an amountof a compound or composition sufficient to prevent, treat, inhibit,reduce, ameliorate or eliminate one or more causes, symptoms, orcomplications of a disease such as a cancer.

The term “subject” includes animals, including mammals and humans,particularly humans.

The term “prodrug” and equivalent expressions refer to agents which canbe converted in vitro or in vivo directly or indirectly to an activeform (see, e.g., R. B. Silverman, 1992, “The Organic Chemistry of DrugDesign and Drug Action,” Academic Press, Chap. 8; Bundgaard, Hans;Editor. Neth. (1985), “Design of Prodrugs”. 360 pp. Elsevier, Amsterdam;Stella, V.; Borchardt, R.; Hageman, M.; Oliyai, R.; Maag, H.; Tilley, J.(Eds.) (2007), “Prodrugs: Challenges and Rewards, XVIII, 1470 p.Springer). Prodrugs can be used to alter the bio-distribution (e.g., toallow agents which would not typically enter the reactive site of aprotease) or the pharmacokinetics for a particular agent. A wide varietyof groups have been used to modify compounds to form prodrugs, forexample, esters, ethers, phosphates, etc. When a prodrug is administeredto a subject, the group is cleaved, enzymatically or non-enzymatically,reductively, oxidatively, or hydrolytically, or otherwise to reveal theactive form. As used herein, “prodrug” includes pharmaceuticallyacceptable salts or esters thereof, or pharmaceutically acceptablesolvates or chelates as well as crystalline forms of any of theforegoing.

Prodrugs are frequently, although not necessarily, pharmacologicallyinactive until converted to the active form. “Inactive” prodrugs arepharmacologically inactive medications that are metabolized into anactive form within the body. For example, instead of administering adrug directly, a corresponding prodrug might be used instead to improvehow a medicine is absorbed, distributed, metabolized, and excreted(ADME) (for examples, see Malhotra, B., et al., “The design anddevelopment of fesoterodine as a prodrug of 5-hydroxymethyl tolterodine(5-HMT), the active metabolite of tolterodine”, Curr. Med. Chem., 2009,16 (33): 4481-9; and Stella, V. J., et al, “Prodrugs. Do they haveadvantages in clinical practice?”. Drugs, 1985. 29 (5): 455-73). Aprodrug may be used to improve how selectively a drug interacts withcells or processes that are not its intended target. This can reduceadverse or unintended effects of a drug, especially important intreatments like chemotherapy, which can have severe unintended andundesirable side effects. For example, Tenofovir alafenamide (TAF), anovel prodrug of tenofovir, was developed to deliver enhanced antiviralpotency and reduced systemic toxicities (Byrne, R., et al, Therap. Adv.Gastroenterol., 2018, 11:1-12).

The term “ester” refers to compounds that can be represented by theformula RCOOR (carboxylic ester) or the formula RSO3R′ (sulfonateester), usually respectively formed by the reaction between a carboxylicor a sulfonic acid and an alcohol usually with the elimination of water.

The term “amino acid” generally refers to an organic compound comprisingboth a carboxylic acid group and an amine group. The term “amino acid”includes both “natural” and “unnatural” or “non-natural” amino acids.Additionally, the term amino acid includes O-alkylated and N-alkylatedamino acids, as well as amino acids having nitrogen or oxygen-containingside chains (such as Lys, Cys, or Ser) in which the nitrogen or oxygenatom has been acylated or alkylated. Amino acids may be pure L or Disomers or mixtures of L and D isomers, including (but not limited to)racemic mixtures.

The term “natural amino acid” and equivalent expressions refer toL-amino acids commonly found in naturally-occurring proteins. Examplesof natural amino acids include, without limitation, alanine (Ala),cysteine (Cys), aspartic acid (Asp), glutamic acid (Glu), phenylalanine(Phe), glycine (Gly), histidine (His), isoleucine (Ile), lysine (Lys),leucine (Leu), methionine (Met), asparagine (Asn), proline (Pro),glutamine (Gln), arginine (Arg), serine (Ser), threonine (Thr), valine(Val), tryptophan (Trp), tyrosine (Tyr), β-alanine (β-Ala), andγ-aminobutyric acid (GABA).

The term “unnatural amino acid” refers to any derivative of a naturalamino acid including D forms, and α- and β-amino acid derivatives. Theterms “unnatural amino acid” and “non-natural amino acid” are usedinterchangeably herein. It is noted that certain amino acids, e.g.,hydroxyproline, that are classified as a non-natural amino acid herein,may be found in nature within a certain organism or a particularprotein. Amino acids with many different protecting groups appropriatefor immediate use in the solid phase synthesis of peptides arecommercially available. In addition to the twenty most common naturallyoccurring amino acids, the following examples of non-natural amino acidsand amino acid derivatives may be used according to the invention(common abbreviations in parentheses): 2-aminoadipic acid (Aad),3-aminoadipic acid (β-Aad), 2-aminobutyric acid (2-Abu),α,β-dehydro-2-aminobutyric acid (8-AU), 1-aminocyclopropane-1-carboxylicacid (ACPC), aminoisobutyric acid (Aib), 3-aminoisobutyric acid (β-Aib),2-amino-thiazoline-4-carboxylic acid, 5-aminovaleric acid (5-Ava),6-aminohexanoic acid (6-Ahx), 2-aminoheptanoic acid (Ahe),8-aminooctanoic acid (8-Aoc), 11-aminoundecanoic acid (11-Aun),12-aminododecanoic acid (12-Ado), 2-aminobenzoic acid (2-Abz),3-aminobenzoic acid (3-Abz), 4-aminobenzoic acid (4-Abz),4-amino-3-hydroxy-6-methylheptanoic acid (Statine, Sta), aminooxyaceticacid (Aoa), 2-aminotetraline-2-carboxylic acid (ATC),4-amino-5-cyclohexyl-3-hydroxypentanoic acid (ACHPA),para-aminophenylalanine (4-NH2-Phe), 2-aminopimelic acid (Apm),biphenylalanine (Bip), para-bromophenylalanine (4-Br-Phe),ortho-chlorophenylalanine (2-C1-Phe), meta-chlorophenylalanine(3-C1-Phe), para-chlorophenylalanine (4-C1-Phe), meta-chlorotyrosine(3-C1-Tyr), para-benzoylphenylalanine (Bpa), tert-butylglycine (TLG),cyclohexylalanine (Cha), cyclohexylglycine (Chg), desmosine (Des),2,2-diaminopimelic acid (Dpm), 2,3-diaminopropionic acid (Dpr),2,4-diaminobutyric acid (Dbu), 3,4-dichlorophenylalanine (3,4-C1-2-Phe),3,4-difluororphenylalanine (3,4-F2-Phe), 3,5-diiodotyrosine(3,5-I2-Tyr), N-ethylglycine (EtGly), N-ethylasparagine (EtAsn),ortho-fluorophenylalanine (2-F-Phe), meta-fluorophenylalanine (3-F-Phe),para-fluorophenylalanine (4-F-Phe), meta-fluorotyrosine (3-F-Tyr),homoserine (Hse), homophenylalanine (Hfe), homotyrosine (Htyr),hydroxylysine (Hyl), allo-hydroxylysine (aHyl), 5-hydroxytryptophan(5-OH-Trp), 3- or 4-hydroxyproline (3- or 4-Hyp), para-iodophenylalanine(4-I-Phe), 3-iodotyrosine (3-I-Tyr), indoline-2-carboxylic acid (Idc),isodesmosine (Ide), allo-isoleucine (a-Ile), isonipecotic acid (Inp),N-methylisoleucine (Melle), N-methyllysine (MeLys), meta-methyltyrosine(3-Me-Tyr), N-methylvaline (MeVal), 1-naphthylalanine (1-Nal),2-naphthylalanine (2-Nal), para-nitrophenylalanine (4-NO2-Phe),3-nitrotyrosine (3-NO2-Tyr), norleucine (Nle), norvaline (Nva),ornithine (Orn), ortho-phosphotyrosine (H2PO3-Tyr),octahydroindole-2-carboxylic acid (Oic), penicillamine (Pen),pentafluorophenylalanine (F5-Phe), phenylglycine (Phg), pipecolic acid(Pip), propargylglycine (Pra), pyroglutamic acid (PGLU), sarcosine(Sar), tetrahydroisoquinoline-3-carboxylic acid (Tic), thienylalanine,and thiazolidine-4-carboxylic acid (thioproline, Th).

For compounds provided herein, it is intended that, in some embodiments,salts thereof are also encompassed, including pharmaceuticallyacceptable salts. Those skilled in the art will appreciate that manysalt forms (e.g., TFA salt, tetrazolium salt, sodium salt, potassiumsalt, etc,) are possible; appropriate salts are selected based onconsiderations known in the art. The term “pharmaceutically acceptablesalt” refers to salts prepared from pharmaceutically acceptablenon-toxic acids or bases including inorganic acids and bases and organicacids and bases. For example, for compounds that contain a basicnitrogen, salts may be prepared from pharmaceutically acceptablenon-toxic acids including inorganic and organic acids. Suitablepharmaceutically acceptable acid addition salts for the compounds of thepresent invention include without limitation acetic, benzenesulfonic(besylate), benzoic, camphorsulfonic, citric, ethenesulfonic, fumaric,gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic,maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic,pantothenic, phosphoric, succinic, sulfuric, tartaric acid,p-toluenesulfonic, and the like. When the compounds contain an acidicside chain, suitable pharmaceutically acceptable base addition salts forthe compounds of the present invention include without limitationmetallic salts made from aluminum, calcium, lithium, magnesium,potassium, sodium and zinc or organic salts made from lysine,N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine,ethylenediamine, meglumine (N-methylglucamine), and procaine.

Compositions

Compounds are generally administered in the form of a pharmaceuticalcomposition (e.g., formulation) comprising at least one active compoundof the present technology together with one or more pharmaceuticallyacceptable carriers, adjuvants, excipients, diluents, fillers, buffers,stabilisers, preservatives, lubricants, or other materials well known tothose skilled in the art, and optionally other therapeutic orprophylactic agents. Thus, there are further provided pharmaceuticalcompositions, and methods of making a pharmaceutical compositioncomprising admixing at least one active compound, as defined above,together with one or more pharmaceutically acceptable carriers,excipients, buffers, adjuvants, stabilizers, or other materials, asdescribed herein.

Pharmaceutical compositions can be in any form suitable for oral,parenteral, topical, intranasal, ophthalmic, otic, rectal,intra-vaginal, or transdermal administration. Where the compositions areintended for parenteral administration, they can be formulated forintravenous, intramuscular, intraperitoneal, subcutaneous administrationor for direct delivery into a target organ or tissue by injection,infusion or other means of delivery. In one particular embodiment, thepharmaceutical composition is in a form suitable for intravenous (i.v.)administration, for example by injection or infusion. In anotherparticular embodiment, the pharmaceutical composition is in a formsuitable for subcutaneous (s.c.) administration.

Pharmaceutical dosage forms suitable for oral administration include,for example and without limitation, tablets, capsules, caplets, pills,lozenges, syrups, solutions, powders, granules, elixirs and suspensions,sublingual tablets, wafers or patches and buccal patches.

Pharmaceutical compositions containing compounds provided herein can beformulated in accordance with known techniques, see for example,Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton,Pa., USA.

In some embodiments, compositions can contain a unit dosage of activecompound together with an inert diluent or carrier such as a sugar orsugar alcohol, eg; lactose, sucrose, sorbitol or mannitol; and/or anon-sugar derived diluent such as sodium carbonate, calcium phosphate,calcium carbonate, or a cellulose or derivative thereof such as methylcellulose, ethyl cellulose, hydroxypropyl methyl cellulose, and starchessuch as corn starch. Tablets may also contain such standard ingredientsas binding and granulating agents such as polyvinylpyrrolidone,disintegrants (e.g. swellable crosslinked polymers such as crosslinkedcarboxymethylcellulose), lubricating agents (e.g. stearates),preservatives (e.g. parabens), antioxidants (e.g. BHT), buffering agents(for example phosphate or citrate buffers), and effervescent agents suchas citrate/bicarbonate mixtures. Such excipients are well-known.

Capsule formulations may be of the hard gelatin or soft gelatin varietyand can contain the active component in solid, semi-solid, or liquidform. Gelatin capsules can be formed from animal gelatin or synthetic orplant derived equivalents thereof.

Solid dosage forms (tablets, capsules, etc.) can be coated or un-coated,but typically have a coating, for example a protective film coating(e.g., a wax or varnish) or a release controlling coating. The coating(e.g. a Eudragit™ type polymer) can be designed to release the activecomponent at a desired location within the gastrointestinal tract. Thus,the coating can be selected so as to degrade under certain pH conditionswithin the gastrointestinal tract, thereby selectively release thecompound in the stomach or in the ileum or duodenum.

Instead of, or in addition to, a coating, the compound can be presentedin a solid matrix comprising a release controlling agent, for example arelease delaying agent which may be adapted to selectively release thecompound under conditions of varying acidity or alkalinity in thegastrointestinal tract. Alternatively, the matrix material or releaseretarding coating can take the form of an erodible polymer (e.g., amaleic anhydride polymer) which is substantially continuously eroded asthe dosage form passes through the gastrointestinal tract. As a furtheralternative, the active compound can be formulated in a delivery systemthat provides osmotic control of the release of the compound. Osmoticrelease and other delayed release or sustained release formulations maybe prepared in accordance with methods well known to those skilled inthe art.

Compositions for topical use include ointments, creams, sprays, patches,gels, liquid drops and inserts (for example, intraocular inserts). Suchcompositions can be formulated in accordance with known methods.

Compositions for parenteral administration are typically presented assterile aqueous or oily solutions or fine suspensions, or may beprovided in finely divided sterile powder form for making upextemporaneously with sterile water for injection.

Examples of formulations for rectal or intra-vaginal administrationinclude pessaries and suppositories which may be, for example, formedfrom a shaped moldable or waxy material containing the active compound.

Compositions for administration by inhalation may take the form ofinhalable powder compositions or liquid or powder sprays, and can beadministrated in standard form using powder inhaler devices or aerosoldispensing devices. Such devices are well known. For administration byinhalation, the powdered formulations typically comprise the activecompound together with an inert solid powdered diluent such as lactose.

Compounds may also be presented in unit dosage form and, as such, willtypically contain sufficient compound to provide a desired level ofbiological activity. The phrase “unit dosage form” refers to physicallydiscrete units, each unit containing a predetemlined amount of theactive compound, either alone or in combination with one or moreadditional agents, sufficient to produce the desired effect. It will beappreciated that the parameters of a unit dosage form will depend on theparticular agent(s) and the effect to be achieved.

In some embodiments, the pharmaceutical composition is provided in asingle-use container (e.g., a single-use vial, ampoule, syringe, orautoinjector, whereas a multi-use container (e.g., a multi-use vial) isprovided in other embodiments.

In some embodiments, a compound may be administered (e.g., orally) atdosage levels of about 0.01 mg/kg to about 50 mg/kg, or about 1 mg/kg toabout 25 mg/kg, of subject body weight per day, one or more times a day,to obtain the desired therapeutic effect. For administration of an oralagent, the compositions can be provided in the form of tablets, capsulesand the like containing from 1.0 to 1000 milligrams of the activeingredient, particularly 1, 3, 5, 10, 15, 20, 25, 50, 75, 100, 150, 200,250, 300, 400, 500, 600, 750, 800, 900, or 1000 milligrams of the activeingredient. For example, a formulation intended for oral administrationmay contain from 0.1 milligrams to 2 grams of active ingredient, moreusually from 10 milligrams to 1 gram, for example, from 50 milligrams to500 milligrams.

In some embodiments, there is provided a composition comprising acompound as described herein and at least one component comprising apharmaceutically acceptable carrier, diluent, adjuvant, excipient, orvehicle, such as a preserving agent, a filler, a disintegrating agent, awetting agent, an emulsifying agent, a suspending agent, a sweeteningagent, a flavoring agent, a perfuming agent, an antibacterial agent, anantifungal agent, a lubricating agent, or a dispensing agent.

In an embodiment, there is provided a pharmaceutical compositioncomprising a compound of the invention, e.g., a compound of Formula I,or a pharmaceutically acceptable salt, ester, or solvate thereof, and apharmaceutically acceptable carrier. In an embodiment, there is provideda pharmaceutical composition comprising a compound in Table 1, or apharmaceutically acceptable salt or ester thereof, and apharmaceutically acceptable carrier. In another embodiment, there isprovided a pharmaceutical composition comprising a compound of Formula Ior a compound in Table 1, or a pharmaceutically acceptable salt or esterthereof, and a pharmaceutically acceptable carrier.

In another embodiment, compounds and/or compositions of the inventionare administered to a subject via various routes, including for exampleand without limitation, intravenous (i.v.) administration, oral (p.o.)administration, intragastric (i.g.) administration, intraperitoneal(i.p.) administration, intramuscular (i.m.) administration, subcutaneous(s.c.) administration, parenteral administration, etc., for deliveringthe compound effectively.

Methods of Use

Compounds provided herein inhibit cyclin dependent kinases, e.g., one ormore cyclin dependent kinase selected from CDK1, CDK2, CDK3, CDK4, CDK5,CDK6, CDK7 and CDK9, and/or glycogen synthase kinase-3 (GSK3). By meansof their activity in modulating or inhibiting CDK kinases and glycogensynthase kinase, compounds are expected to be useful in providing ameans of arresting, or recovering control of, the cell cycle inabnormally dividing cells. It is therefore anticipated that thecompounds will prove useful in treating or preventing proliferativedisorders such as cancers. It is also envisaged that the compounds ofthe invention may be useful in treating conditions such as, for exampleand without limitation, viral infections, type II or non-insulindependent diabetes mellitus, autoimmune diseases, head trauma, stroke,epilepsy, neurodegenerative diseases such as Alzheimer's, motor neurondisease, progressive supranuclear palsy, corticobasal degeneration andPick's disease. In particular embodiments, compounds are useful fortreatment of viral infections, autoimmune diseases and/orneurodegenerative diseases.

CDKs play a role in the regulation of the cell cycle, apoptosis,transcription, differentiation and CNS function. Therefore, CDKinhibitors could be useful in the treatment of diseases in which thereis a disorder of proliferation, apoptosis or differentiation, such ascancer and tumors. Examples of cancers which may be inhibited or treatedin accordance with the present technology include, but are not limitedto, a carcinoma, for example a carcinoma of the bladder, breast, colon(e.g., colorectal carcinomas such as colon adenocarcinoma and colonadenoma), kidney, epidermis, liver, lung, for example adenocarcinoma,small cell lung cancer and non-small cell lung carcinomas, oesophagus,gall bladder, ovary, pancreas e.g., exocrine pancreatic carcinoma,stomach, cervix, thyroid, prostate, or skin, for example squamous cellcarcinoma; a hematopoietic tumour of lymphoid lineage, for exampleleukemia, acute lymphocytic leukemia, B-cell lymphoma, T-cell lymphoma,Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma, orBurkett's lymphoma; a hematopoietic tumour of myeloid lineage, forexample acute and chronic myelogenous leukemias, myelodysplasticsyndrome, or promyelocytic leukemia; thyroid follicular cancer; a tumourof mesenchymal origin, for example fibrosarcoma or habdomyosarcoma, atumour of the central or peripheral nervous system, for exampleastrocytoma, neuroblastoma, glioma or schwannoma; melanoma; seminoma;teratocarcinoma; osteosarcoma; xeroderma pigmentosum; keratoctanthoma;thyroid follicular cancer; or Kaposi's sarcoma.

The cancers to be treated or inhibited may be cancers which aresensitive to inhibition of any one or more cyclin dependent kinaseselected from CDK1, CDK2, CDK3, CDK4, CDK5, CDK6, CDK7, and CDK9, forexample, one or more CDK kinases selected from CDK1, CDK2, CDK4, CDK5,CDK6, and CDK9, e.g., CDK1 and/or CDK2, CDK4 and/or CDK6, etc.

CDKs are also known to play a role in apoptosis, proliferation,differentiation and transcription and therefore CDK inhibitors couldalso be useful in the treatment of the following diseases other thancancer: viral infections, for example herpes virus, pox virus,Epstein-Barr virus, Sindbis virus, adenovirus, HIV, HPV, HCV and HCMV;prevention of AIDS development in HIV-infected individuals; chronicinflammatory diseases, for example systemic lupus erythematosus,autoimmune mediated glomerulonephritis, rheumatoid arthritis, psoriasis,inflammatory bowel disease, and autoimmune diabetes mellitus;cardiovascular diseases for example cardiac hypertrophy, restenosis,atherosclerosis; neurodegenerative disorders, for example Alzheimer'sdisease, AIDS-related dementia, Parkinson's disease, amyotropic lateralsclerosis, retinitis pigmentosa, spinal muscular atropy and cerebellardegeneration; glomerulonephritis; myelodysplastic syndromes, ischemicinjury associated myocardial infarctions, stroke and reperfusion injury,arrhythmia, atherosclerosis, toxin-induced or alcohol related liverdiseases, haematological diseases, for example, chronic anemia andaplastic anemia; degenerative diseases of the musculoskeletal system,for example, osteoporosis and arthritis, aspirin-sensitiverhinosinusitis, cystic fibrosis, multiple sclerosis, kidney diseases andcancer pain.

Thus, in the pharmaceutical compositions, uses or methods of thisinvention for treating a disease or condition comprising abnormal cellgrowth, the disease or condition comprising abnormal cell growth in oneembodiment is a cancer. One group of cancers includes human breastcancers (e.g. primary breast tumours, node-negative breast cancer,invasive duct adenocarcinomas of the breast, non-endometrioid breastcancers); and mantle cell lymphomas. In addition, other cancers arecolorectal and endometrial cancers. Another sub-set of cancers includesbreast cancer, ovarian cancer, colon cancer, prostate cancer,oesophageal cancer, squamous cancer and non-small cell lung carcinomas.

It is contemplated that compounds and compositions provided herein maybe used for the prevention or treatment of any disease state orcondition mediated by a cyclin dependent kinase (CDK) and/or glycogensynthase kinase-3 (GSK-3). As used herein, the expression “disease stateor condition mediated by a cyclin dependent kinase (CDK) and/or glycogensynthase kinase-3 (GSK-3)” refers to any disease or condition mentionedherein for which inhibition or modulation of a CDK and/or GSK-3 would beexpected to provide a therapeutic or prophylactic benefit in a subjectin need thereof.

In some embodiments, the active compound or composition is administeredto a subject in need thereof (for example, a human or animal patient) inan amount sufficient to achieve the desired therapeutic effect.Compounds and compositions are typically administered in amounts thatare therapeutically or prophylactically useful and which generally arenon-toxic. However, in certain situations (for example in the case oflife threatening diseases), the benefits of administering a compound orcomposition may outweigh the disadvantages of any toxic effects or sideeffects, in which case it may be considered desirable to administercompounds in amounts that are associated with a degree of toxicity.

A typical daily dose of a compound can be in the range from 100picograms to 100 milligrams per kilogram of body weight, more typically5 nanograms to 25 milligrams per kilogram of bodyweight, and moreusually 10 nanograms to 15 milligrams per kilogram (e.g., 10 nanogramsto 10 milligrams) per kilogram of bodyweight, although higher or lowerdoses may be administered where required. Ultimately, the quantity ofcompound administered and the type of composition used will becommensurate with the nature of the disease or physiological conditionbeing treated and will be at the discretion of the physician.

Compounds and compositions provided herein can be administered as thesole therapeutic agent or they can be administered in combinationtherapy with one of more other compounds for treatment of a particulardisease state, for example a neoplastic disease such as a cancer.Examples of other therapeutic agents that may be administered together(whether concurrently or at different time intervals) with the compoundsand compositions provided herein include but are not limited to:topoisomerase inhibitors, alkylating agents, antimetabolites, DNAbinders and microtubule inhibitors (tubulin targeting agents), such ascisplatin, cyclophosphamide, doxorubicin, irinotecan, fludarabine,flavopiridol, SFU, taxanes, mitomycin C or other chemotherapeuticagents, immune checkpoint inhibitors, or radiotherapy. Alternatively,the compounds and compositions provided herein can be administered in acombination therapy with monoclonal antibodies or signal transductioninhibitors. Compounds and compositions may also be administered incombination with bone marrow transplantation, peripheral blood stem celltransplantation, or other types of transplantation therapy.

In some embodiments, compounds and compositions may be administered incombination with immune checkpoint inhibitors. The blockade of immunecheckpoints, which results in the amplification of antigen-specific Tcell responses, has been shown to be a promising approach in humancancer therapeutics. Non-limiting examples of immune checkpoints(ligands and receptors), some of which are selectively upregulated invarious types of tumor cells, that are candidates for blockade includePD1 (programmed cell death protein 1); PDL1 (PD1 ligand); BTLA (B and Tlymphocyte attenuator); CTLA4 (cytotoxic T-lymphocyte associated antigen4); TIM3 (T-cell membrane protein 3); LAG3 (lymphocyte activation gene3); A2aR (adenosine Ata receptor A2aR); and Killer Inhibitory Receptors.Non-limiting examples of immune checkpoint inhibitors includeipulimumab, nivolumab and lambrolizumab.

In other embodiments, there are provided methods for treating cancer ina subject, comprising administering to the subject a therapeuticallyeffective amount of at least compound or composition of the presentdisclosure and at least one chemotherapeutic agent, such agentsincluding, but not limited to alkylating agents (e.g., nitrogen mustardssuch as chlorambucil, cyclophosphamide, isofamide, mechlorethamine,melphalan, and uracil mustard; aziridines such as thiotepa;methanesulphonate esters such as busulfan; nucleoside analogs (e.g.,gemcitabine); nitroso ureas such as carmustine, lomustine, andstreptozocin; topoisomerase 1 inhibitors (e.g., irinotecan); platinumcomplexes such as cisplatin and carboplatin; bioreductive alkylatorssuch as mitomycin, procarbazine, dacarbazine and altretamine); DNAstrand-breakage agents (e.g., bleomycin); topoisomerase II inhibitors(e.g., amsacrine, dactinomycin, daunorubicin, idarubicin, mitoxantrone,doxorubicin, etoposide, and teniposide); DNA minor groove binding agents(e.g., plicamydin); antimetabolites (e.g., folate antagonists such asmethotrexate and trimetrexate; pyrimidine antagonists such asfluorouracil, fluorodeoxyuridine, CB3717, azacitidine, cytarabine, andfloxuridine; purine antagonists such as mercaptopurine, 6-thioguanine,fludarabine, pentostatin; asparginase; and ribonucleotide reductaseinhibitors such as hydroxyurea); tubulin interactive agents (e.g.,vincristine, estramustine, vinblastine, docetaxol, epothilonederivatives, and paclitaxel); hormonal agents (e.g., estrogens;conjugated estrogens; ethinyl estradiol; diethylstilbesterol;chlortrianisen; idenestrol; progestins such as hydroxyprogesteronecaproate, medroxyprogesterone, and megestrol; and androgens such astestosterone, testosterone propionate, fluoxymesterone, andmethyltestosterone); adrenal corticosteroids (e.g., prednisone,dexamethasone, methylprednisolone, and prednisolone); leutinizinghormone releasing agents or gonadotropin-releasing hormone antagonists(e.g., leuprolide acetate and goserelin acetate); and antihormonalantigens (e.g., tamoxifen, antiandrogen agents such as flutamide; andantiadrenal agents such as mitotane and aminoglutethimide). There isalso provided the use of the compounds and compositions in combinationwith other agents known in the art (e.g., arsenic trioxide) and otherchemotherapeutic agents that may be developed in the future.

In some embodiments drawn to methods of treating cancer, theadministration of a therapeutically effective amount of a compound orcomposition in combination with at least one chemotherapeutic agentresults in a cancer survival rate greater than the cancer survival rateobserved by administering either agent alone. In further embodimentsdrawn to methods of treating cancer, the administration of atherapeutically effective amount of a compound or composition incombination with at least one chemotherapeutic agent results in areduction of tumor size or a slowing of tumor growth greater thanreduction of the tumor size or slowing of tumor growth observed byadministration of either agent alone.

In further embodiments, there are provided methods for treating orpreventing cancer in a subject, comprising administering to the subjecta therapeutically effective amount of at least one CDK and/or GSK3inhibitor compound or composition and at least one signal transductioninhibitor (STI). In a particular embodiment, the at least one STI isselected from the group consisting of bcr/abl kinase inhibitors,epidermal growth factor (EGF) receptor inhibitors, her-2/neu receptorinhibitors, and farnesyl transferase inhibitors (FTIs).

In other embodiments, there are provided methods of augmenting therejection of tumor cells in a subject comprising administering acompound or composition in conjunction with at least onechemotherapeutic agent and/or radiation therapy, wherein the resultingrejection of tumor cells is greater than that obtained by administeringeither the compound, the chemotherapeutic agent or the radiation therapyalone.

In further embodiments, there are provided methods for treating cancerin a subject, comprising administering to the subject a therapeuticallyeffective amount of at least one CDK and/or GSK3 inhibitor and at leastone immunomodulator other than a CDK inhibitor. It should be understoodthat, as used herein, a “CDK and/or GSK3 inhibitor” refers to compoundsprovided herein, e.g., a compound of Formula I, a compound of Table 1,or a pharmaceutically acceptable salt or ester thereof, and topharmaceutical compositions thereof.

In some embodiments, there are provided methods of treating orpreventing a disease state or condition mediated by a cyclin dependentkinase (CDK) and/or glycogen synthase kinase-3 (GSK-3) in a subject inneed thereof, comprising administering a therapeutically effectiveamount of at least one CDK and/or GSK3 inhibitor or a pharmaceuticalcomposition thereof to the subject, such that the CDK and/or GSK-3associated disease, disorder or condition is treated or prevented in thesubject.

For the case of CDK inhibitors combined with other therapies, the two ormore treatments may be given in individually varying dose schedules andvia different routes.

In some embodiments, there are provided methods of inhibition ormodulation of a cyclin dependent kinase (CDK) and/or glycogen synthasekinase-3 (GSK-3) in a subject, comprising administering an effectiveamount of at least one CDK and/or GSK3 inhibitor or a pharmaceuticalcomposition thereof to the subject, such that the CDK and/or GSK-3 isinhibited or modulated in the subject.

Where a compound or composition provided herein is administered incombination therapy with one, two, three, four or more other therapeuticagents (preferably one or two, more preferably one), the compounds canbe administered simultaneously or sequentially. When administeredsequentially, they can be administered at closely spaced intervals (forexample, over a period of 5-10 minutes) or at longer intervals (forexample, 1, 2, 3, 4 or more hours apart, or even longer periods apartwhere required), the precise dosage regimen being commensurate with theproperties of the therapeutic agent(s).

Compounds and compositions provided herein may also be administered inconjunction with non-chemotherapeutic treatments such as, withoutlimitation, radiotherapy, photodynamic therapy, gene therapy, surgery,transplantation, immune checkpoint inhibitor therapy, and controlleddiets.

Kits

There are also provided herein kits comprising a compound or compositionof the present technology. Kits are generally in the form of a physicalstructure housing various components and may be used, for example, inpracticing the methods provided herein. For example, a kit may includeone or more compound disclosed herein (provided in, e.g., a sterilecontainer), which may be in the form of a pharmaceutical compositionsuitable for administration to a subject. The compound can be providedin a form that is ready for use (e.g., a tablet or capsule) or in a formrequiring, for example, reconstitution or dilution (e.g., a powder)prior to administration. When the compounds are in a form that needs tobe reconstituted or diluted by a user, the kit may also include diluents(e.g., sterile water), buffers, pharmaceutically acceptable excipients,and the like, packaged with or separately from the compounds. Whencombination therapy is contemplated, the kit may contain severaltherapeutic agents separately or they may already be combined in thekit. Each component of the kit may be enclosed within an individualcontainer, and all of the various containers may be within a singlepackage. A kit of the present invention may be designed for conditionsnecessary to properly maintain the components housed therein (e.g.,refrigeration or freezing).

A kit may also contain a label or packaging insert including identifyinginformation for the components therein and instructions for their use(e.g., dosing parameters, clinical pharmacology of the activeingredient(s), including mechanism of action, pharmacokinetics andpharmacodynamics, adverse effects, contraindications, etc.). Labels orinserts can include manufacturer information such as lot numbers andexpiration dates. The label or packaging insert may be, e.g., integratedinto the physical structure housing the components, contained separatelywithin the physical structure, or affixed to a component of the kit(e.g., an ampule, tube or vial).

EXAMPLES

The present invention will be more readily understood by referring tothe following examples, which are provided to illustrate the inventionand are not to be construed as limiting the scope thereof in any manner.

Unless defined otherwise or the context clearly dictates otherwise, alltechnical and scientific terms used herein have the same meaning ascommonly understood by one of ordinary skill in the art to which thisinvention belongs. It should be understood that any methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of the invention.

Example 1: Preparation of tert-butyl4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(Compound A)

tert-Butyl 4-(4-amino-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(0.6 g, 1.98 mmol, 1.0 eq.) was dissolved in DMF (10 mL), Et₃N (404 mg,4.0 mmol, 2.0 eq.) was added, then 2,6-dichlorobenzoyl chloride (490 mg,2.3 mmol, 1.2 eq.) was added dropwise, The mixture was stirred at roomtemperature for 12 h under N₂ atmosphere, then the mixture wasconcentrated under reduced pressure. The residual material was purifiedby flash column chromatography (silica-gel; eluent, PE:EA, 1:2 to 1:1)to afford compound A (720 mg, 75%): ¹H NMR (CD₃OD, 500 MHz) δ ppm1.44-1.53 (m, 11H), 1.90 (d, J=10 Hz, 2H), 2.91 (s, 2H), 3.99-4.09 (m,3H), 4.6 (s, 1H), 7.41-7.53 (m, 3H), 8.33 (s, 1H); ¹³C NMR (CD₃OD, 125MHz): δ ppm 37.57, 40.50, 55.32, 88.13, 130.18, 130.99, 137.92, 140.74,141.38, 142.37, 144.85, 163.36, 169.77, 172.07; m/z (ESI⁻) 480.0 (M−H).

Example 2: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(4-((2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)oxy)butyl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(Compound 2)

4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidemethanesulfonate (240 mg, 0.5 mmol, 1.0 eq.) was dissolved in DMF (10mL), Et₃N (101 mg, 1.0 mmol, 2.0 eq.) was added, followed by dropwiseaddition of 7-(4-bromobutoxy)-3,4-dihydro-2(1H)-quinolinone (163 mg,0.55 mmol, 1.1 eq.). The mixture was stirred at room temperature for 12h under N₂ atmosphere, and then concentrated under reduced pressure. Theresidual material was purified by flash column chromatography(silica-gel; eluent: MeOH:DCM, 1:30 to 1:20), affording compound 2 (120mg, 40%): ¹H NMR (DMSO-d₆, 500 MHz) δ ppm 1.51-1.54 (m, 2H), 1.60-1.70(m, 6H), 1.88 (t, J=10 Hz, 2H), 2.28 (t, J=5 Hz, 2H), 2.40 (t, J=5 Hz,2H), 2.77 (t, J=5 Hz, 2H), 2.83 (d, J=10 Hz, 2H), 3.70 (s, 1H), 3.89 (t,J=5 Hz, 2H), 6.42 (s, 1H), 6.47 (dd, J=10 Hz, 5 Hz, 1H), 7.03 (d, J=10Hz, 1H), 7.51-7.54 (m, 1H), 7.58 (d, J=5 Hz, 2H), 8.27 (s, 1H), 8.34 (s,1H), 9.95 (s, 1H), 10.17 (s, 1H), 13.39 (s, 1H); ¹³C NMR (DMSO-d₆, 125MHz) δ ppm 23.09, 24.00, 26.67, 30.76, 31.29, 46.32, 52.38, 57.42,67.31, 101.70, 107.55, 115.43, 121.48, 128.36, 128.41, 131.25, 131.86,132.71, 135.37, 139.17, 157.87, 160.31, 162.47, 170.26; m/z (ESI⁻) 599.1(M+H).

Example 3: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(L-valyl)piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (Compound 3)

4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidemethanesulfonate (480 mg, 1.0 mmol, 1.0 eq.) was dissolved in a mixtureof DMF (7 mL) and Et₃N (220 mg, 2.0 mmol, 2.0 eq.), followed by additionof 2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-valinate (320 mg,1.0 mmol, 1.0 eq.). The mixture was stirred at room temperature for 12 hunder N₂ atmosphere, and then concentrated under reduced pressure. Theresidual material was purified by flash column chromatography(silica-gel; eluent: PE:EA, 1:1), giving4-(2,6-dichlorobenzamido)-N-(1-(N-Boc-L-valy)piperidin-4-yl)-1H-pyrazole-3-carboxamide(516 mg, 89%). The above obtained4-(2,6-dichlorobenzamido)-N-(1-(L-valyl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(516 mg, 0.9 mmol, 1.0 eq.) was dissolved in dioxane (5 mL), followed byaddition of 4 M HCl in dioxane (2 mL) dropwise. The mixture was stirredat room temperature for 5 h, followed by concentration under reducedpressure. The residual material was purified by flash columnchromatography (silica-gel; eluent: DCM and MeOH, 20:1), affordingcompound 3 (210 mg, 45%): ¹H NMR (D₂O, 500 MHz) δ ppm 0.98 (t, J=4 Hz,3H), 1.08 (dd, J=8 Hz, 4 Hz, 3H), 1.55-1.61 (m, 2H), 2.03-2.07 (m, 2H),2.22 (s, 1H), 3.01 (t, J=8 Hz, 1H), 3.35 (s, 1H), 3.94 (s, 1H), 4.09 (s,1H), 4.36 (dd, J=12 Hz, 4 Hz, 2H), 7.47 (s, 3H), 8.30 (d, J=8 Hz, 1H);¹³C NMR (D₂O, 125 MHz) δ ppm 15.75, 18.10, 29.37, 30.49, 31.17, 41.50,44.67, 45.94, 55.41, 119.80, 123.28, 128.18, 131.46, 131.87, 133.82,134.26, 163.02, 164.29, 167.88; m/z (ESI⁻) 480.8 (M+H).

Example 4: Preparation of4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-1-(dodecyloxymethyl)pyrazole-3-carboxamidehydrochloride (Compound 4)

Dodecanoic acid (2.0 g, 10.0 mmol, 1.0 eq.) was dissolved in DCM-H₂O(1:1, 40 mL), followed by addition of chloromethyl sulfurochloridate(1.2 mL, 11.5 mmol, 1.15 eq.), Na₂CO₃ (4.1 g, 40 mmol, 4.0 eq) and TBAB(320 mg, 1.0 mmol, 0.1 eq.), subsequently. The mixture was stirred atroom temperature for 12 h, diluted with DCM (100 mL) and H₂O (100 mL).The organic layer was separated, washed with brine (50 mL), andconcentrated under reduced pressure. The residual material was purifiedby flash column chromatography (silica-gel; eluent: pet-ether), givingchloromethyl dodecanoate (2.0 g, 80%). Compound A (530 mg, 1.1 mmol, 1.0eq.) was dissolved in CH₃CN (10 mL), followed by addition ofchloromethyl dodecanoate (273 mg, 1.1 mmol, 1.0 eq.) and NaHCO₃ (185 mg,2.2 mmol, 2.0 eq), subsequently. The mixture was stirred for 48 h undernitrogen and heated to 60° C., and then concentrated under reducedpressure. The residual material was purified by flash columnchromatography (silica-gel; eluent: PE:EA, 2:1) to afford tert-butyl4-(4-(2,6-dichlorobenzamido)-1-((dodecanoyloxy)methyl)-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate (190 mg, 25%): ¹H NMR (CDCl₃, 500 MHz) δ ppm0.81 (t, J=10 Hz, 3H), 1.18-1.21 (m, 18H), 1.39 (s, 9H), 1.51-1.60 (m,2H), 1.89 (d, J=5 Hz, 2H), 2.30 (t, J=10 Hz, 2H), 2.80 (t, J=10 Hz, 2H),3.95-4.03 (m, 3H), 5.94 (s, 2H), 6.76 (d, J=5 Hz, 1H), 7.20-7.28 (m,3H), 8.50 (s, 1H), 9.77 (s, 1H). The above obtained compound (190 mg,0.3 mmol, 1.0 eq.) was dissolved in dioxane (10 mL), followed byaddition of 4 M HCl in dioxane (4 mL). The mixture was stirred at roomtemperature for 12 h and then concentrated under reduced pressure. Theresidual material was purified by flash column chromatography(silica-gel; eluent: DCM:MeOH, 20:1), giving compound 4 (120 mg, 40%):¹H NMR (CD₃OD, 500 MHz): δ ppm 0.87 (t, J=8 Hz, 3H), 1.25 (s, 16H), 1.60(s, 2H). 1.91 (dd, J=12 Hz, 4 Hz, 2H), 2.13 (d, J=8 Hz, 2H), 2.38 (t,J=8 Hz, 2H), 3.10 (t, J=8 Hz, 2H), 3.43 (d, J=8 Hz, 2H), 4.12 (t, J=8Hz, 1H), 6.13 (s, 2H), 7.47 (s, 3H), 8.55 (s, 1H); ¹³C NMR (CD₃OD, 125MHz): δ ppm 14.47, 23.69, 25.74, 29.42, 29.94, 30.31, 30.41, 30.56,30.68, 33.02, 34.63, 44.27, 45.30, 73.93, 124.01, 125.27, 129.48,132.89, 133.34, 135.61, 136.38, 163.16, 164.12, 174.30; m/z (ESI⁺) 594.1(M+H).

Example 5: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(N-glycyl-L-valy)piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (Compound 5)

N-(tert-Butoxycarbonyl)glycyl-L-valine (274 mg, 1.0 mmol, 1.0 eq.) andEt₃N (202 mg, 2.0 mmol, 2.0 eq.) were added to a solution of4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) in DMF (10 mL), followed byaddition of HATU (418 mg, 1.1 mmol, 1.1 eq.). The mixture was stirred atroom temperature for 12 h, and then concentrated under reduced pressure.The residual material was purified by flash column chromatography(silica-gel; eluent, ethyl acetate), giving4-(2,6-dichlorobenzamido)-N-(1-(N-(N-^(t)Boc-glycyl)-L-valyl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(500 mg, 78%). The material thus obtained (500 mg, 1.27 mmol, 1.0 eq.)was dissolved in dioxane (10 mL), followed by addition of 4M HCl indioxane (5 mL). The mixture was stirred at room temperature for 12 h,and then concentrated under reduced pressure. The residual material waspurified by flash column chromatography (silica-gel; eluent: DCM:MeOH,20:1), affording compound 5 (100 mg, 14%): ¹H NMR (D₂O, 500 MHz) δ ppm0.92-0.97 (m, 6H), 1.50 (s, 1H), 1.66 (d, J=8 Hz, 1H), 2.05-2.09 (m,3H), 2.96 (s, 1H), 3.35 (s, 1H), 3.84-3.94 (m, 2H), 4.10 (t, J=12 Hz,2H), 4.35 (d, J=12 Hz, 1H), 4.79 (s, 1H), 7.46 (s, 3H), 8.30 (d, J=8 Hz,1H); ¹³C NMR (CD₃OD, 125 MHz) δ ppm 18.15, 19.84, 31.75, 32.30, 33.09,41.47, 42.32, 45.95, 47.39, 55.66, 122.70, 122.83, 129.38, 132.76,133.21, 134.15, 136.41, 163.13, 164.43, 167.15, 171.41; m/z (ESI⁺) 537.9(M+H).

Example 6: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(3-methylbutanoyl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(Compound 6)

Et₃N (202 mg, 2.0 mmol, 2.0 eq) and 3-methylbutanoic acid (102 mg, 1.0mmol, 1.0 eq.) were added to a solution of4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) in DMF (10 mL), followed byaddition of HATU (418 mg, 1.1 mmol, 1.1 eq.). The mixture was stirred atroom temperature for 12 h, and then concentrated under reduced pressure.The residual material was purified by flash column chromatography(silica-gel; eluent: PE:EA, 2:1), affording compound 6 (380 mg, 82%): ¹HNMR (CD₃OD, 500 MHz) δ ppm 0.97 (dd, J=10 Hz, 5 Hz, 6H), 1.52-1.56 (m,2H), 1.93-2.07 (m, 3H), 2.29 (d, J=10 Hz, 2H), 2.80 (t, J=15 Hz, 1H),3.21 (t, J=15 Hz, 1H), 3.99 (d, J=15 Hz, 1H), 4.08-4.12 (m, 1H), 4.52(d, J=15 Hz, 1H), 7.46-7.52 (m, 3H), 8.35 (s, 1H); ¹³C NMR (CD₃OD, 125MHz) δ ppm 23.02, 23.12, 27.30, 32.60, 33.47, 42.02, 43.09, 46.24,47.78, 122.49, 123.16, 129.64, 132.94, 133.62, 134.70, 136.85, 163.42,164.99, 173.56; m/z (ESI⁺) 466.0 (M+H).

Example 7: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(L-valyl-glycyl)piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (Compound 7)

4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) andN-(tert-butoxycarbonyl)-L-valyl-glycine (274 mg, 1.0 mmol, 1.0 eq.) weredissolved in DMF (10 mL). To the mixture were added Et₃N (202 mg, 2.0mmol, 2.0 eq.) and HATU (418 mg, 1.1 mmol, 1.1 eq). The mixture wasstirred at room temperature for 12 h, concentrated under reducedpressure. The residual material was purified by flash columnchromatography (silica-gel; eluent: PE:EA, 1:1), giving4-(2,6-dichlorobenzamido)-N-(1-(N-Boc-L-valyl-glycyl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(560 mg, 88%). The compound thus obtained (560 mg, 0.88 mmol, 1.0 eq.)was dissolved in dioxane (5 mL), followed by addition of 4M HCl indioxane (5 mL). The mixture was stirred at room temperature for 12 h,and concentrated under reduced pressure. The residual material waspurified by flash column chromatography (silica-gel; eluent: DCM:MeOH,20:1), affording compound 7 (230 mg, 50%): ¹H NMR (CD₃OD, 500 MHz) δ ppm1.08 (d, J=10 Hz, 6H), 1.50-1.69 (m, 2H), 1.95-2.05 (m, 2H), 2.17-2.25(m, 1H), 2.88 (t, J=15 Hz, 1H), 3.23 (t, J=15 Hz, 1H), 3.71 (d, J=10 Hz,1H), 3.90 (d, J=15 Hz, 1H), 4.08-4.26 (m, 3H), 4.46 (d, J=15 Hz, 1H),7.44-7.52 (m, 3H), 8.34 (s, 1H); ¹³C NMR (D₂O, 125 MHz) δ ppm 17.09,17.67, 29.99, 30.63, 31.17, 40.93, 41.45, 43.65, 46.09, 58.79, 120.51,122.98, 128.30, 131.62, 131.86, 133.89, 134.11, 162.99, 163.64, 167.70,169.62; m/z (ESI⁺) 538.0 (M+H).

Example 8: Preparation of4-(2,6-dichlorobenzamido)-N-(1-Boc-piperidin-4-yl)-1-dodecanoyl-1H-pyrazole-3-carboxamide(Compound 8)

Compound A (481 mg, 1.0 mmol, 1.0 eq.) and Et₃N (202 mg, 2.0 mmol, 2.0eq.) were dissolved in DMF (10 mL), then dodecanoyl chloride (219 mg,1.0 mmol, 1.0 eq.) was added. The contents were stirred for 12 h underNitrogen. The mixture was concentrated under reduced pressure. Theresidual material was purified by flash column chromategraphy(silica-gel; eluent: PE:EA, 3:1), affording compound 8 (300 mg, 45%): ¹HNMR (DMSO-d₆, 500 MHz) δ ppm 0.9 (t, J=10 Hz, 3H), 1.29-1.40 (m, 25H),1.55-1,59 (m, 2H), 1.75-1.81 (m, 2H), 1.87-1.91 (m, 2H), 2.85 (s, 2H),3.23 (t, J=10 Hz, 2H), 4.06-4.12 (m, 3H), 7.45-7.52 (m, 3H), 8.91 (s,1H); ¹³C NMR (DMSO-d₆, 125 MHz) δ ppm 14.49, 23.72, 25.20, 28.73, 30.10,30.45, 30.60, 30.71, 32.46, 33.04, 34.12, 48.07, 81.13, 120.44, 125.23,129.50, 132.93, 133.31, 136.23, 138.76, 156.33, 163.33, 163.49, 173.21;m/z (ESI⁻) 662.2 (M−H).

Example 9: Preparation of4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1-(L-valyloxymethyl)-1H-pyrazole-3-carboxamidedihydrochloride (Compound 10)

(tert-Butoxycarbonyl)-L-valine (434 mg, 2.0 mmol, 1.0 eq.) was dissolvedin DCM-H₂O (v/v, 1:1, 10 mL), followed by addition of chloromethylsulfurochloridate (0.24 mL, 2.3 mmol, 1.15 eq.), Na₂CO₃ (850 mg, 8.0mmol, 4.0 eq.), and TBAB (65 mg, 0.2 mmol, 0.1 eq.), subsequently. Themixture was stirred at room temperature for 12 h, diluted with DCM (50mL) and H₂O (50 mL). The organic layer was separated, washed with brine(3×20 mL), and concentrated under reduced pressure. The residualmaterial was purified by flash column chromatography (silica-gel;eluent, pet-ether), giving chloromethylN-(tert-butoxycarbonyl)-L-valinate (480 mg, 90.5%). Compound A (481 mg,1.0 mmol, 1.0 eq.) was dissolved in CH₃CN (10 mL), followed by additionof chloromethyl N-(tert-butoxycarbonyl)-L-valinate (265 mg, 1.0 mmol,1.0 eq.) and NaHCO₃ (168 mg, 2.0 mmol, 2.0 eq.), subsequently. Themixture was stirred for 48 h under nitrogen at 60° C. The mixture wasconcentrated under reduced pressure. The residual material was purifiedby flash column chromatography (silica-gel; eluent: PE:EA, 2:1), giving4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1-(N-Boc-L-valyloxymethyl)-1H-pyrazole-3-carboxamide(450 mg, 63%). This Boc-protected compound (240 mg, 0.5 mmol, 1.0 eq.)was dissolved in dioxane (10 mL), followed by addition of 4M HCl indioxane (0.5 mL). The mixture was stirred at room temperature for 12 hand concentrated under reduced pressure. The residual material waspurified by flash column chromatography (silica-gel; eluent: DCM:MeOH,20:1), affording compound 10 (120 mg, 47%): ¹H NMR (D₂O, 500 MHz) δ ppm0.93 (t, J=10 Hz, 6H), 1.82-1.91 (m, 2H), 2.22 (d, J=10 Hz, 2H),2.30-2.36 (m, 1H), 3.18 (t, J=10 Hz, 2H), 3.52 (d, J=10 Hz, 2H),4.12-4.15 (m, 2H), 6.24 (d, J=10 Hz, 1H), 6.47 (d, J=10 Hz, 1H),7.47-7.54 (m, 3H), 8.58 (s, 1H); ¹³C NMR (D₂O, 125 MHz) δ ppm 16.91,27.79, 29.35, 42.91, 44.21, 57.94, 73.75, 120.78, 126.71, 128.30,128.48, 131.51, 132.17, 133.72, 162.66, 165.30, 168.91; m/z (ESI⁺) 511.1(M+H).

Example 10: Synthesis of sodium(4-(2,6-dichlorobenzamido)-3-(piperidin-4-ylcarbamoyl)-1H-pyrazole-1-methylphosphate disodium salt (Compound 11)

Compound A (481 mg, 1.0 mmol, 1.0 eq.) and di-tert-butyl (chloromethyl)phosphate (258.7 mg, 1.0 mmol, 1.0 eq.) were dissolved in AcNMe₂ (10mL), followed by addition of Cs₂CO₃ (652 mg, 2.0 mmol, 2.0 eq.). Themixture was stirred for 12 h under nitrogen at 40 to 45° C. The mixturewas diluted with DCM (50 mL) and H₂O (50 mL). The organic layer wasseparated, washed with brine (3×20 mL), and concentrated under reducedpressure. The residual material was purified by flash columnchromatography (silica-gel; eluent: PE:Acetone, 3:1), givingdi-tert-butyl(4-(2,6-dichlorobenzamido)-3-(piperidin-4-ylcarbamoyl)-1H-pyrazole-1-methylphosphate (240 mg, 34.1%). The phosphate ester thus obtained (150 mg,0.2 mmol, 1.0 eq.) was dissolved in DCM (2 mL), followed by addition ofCF₃COOH (1 mL). The mixture was stirred for 1 min, concentrated underreduced pressure, and treated with t-BuOMe (5 mL). Solid material wascollected by filtration and dried, giving(4-(2,6-dichlorobenzamido)-3-(piperidin-4-ylcarbamoyl)-1H-pyrazol-1-yl)methyldihydrogen phosphate (75 mg, 76.2%). This(4-(2,6-dichlorobenzamido)-3-(piperidin-4-ylcarbamoyl)-1H-pyrazol-1-yl)methyldihydrogen phosphate (49.1 mg, 0.1 mmol, 1.0 eq.) was dissolved in H₂O(2 mL) and treated with NaOH (8 mg, 0.2 mmol, 2.0 eq.). The mixture werestirred for 0.5 h and lyophilized, affording compound 11 (47 mg, 87.9%):¹H NMR (500 MHz, D₂O) δ ppm 1.53 (d, J=10.5 Hz, 2H), 1.94 (d, J=12.8 Hz,2H), 2.72 (t, J=12.2 Hz, 2H), 3.07 (d, J=12.2 Hz, 2H), 3.90 (s, 1H),5.66 (d, J=7.5 Hz, 2H), 7.37 (d, J=8.4 Hz, 1H), 7.43 (d, J=8.0 Hz, 2H),8.32 (s, 1H); ¹³C NMR (125 MHz, D₂O) δ ppm 30.30, 43.26, 45.70, 75.70,123.45, 125.10, 128.18, 131.30, 131.44, 135.57, 136.54, 163.00, 165.66;m/z (ESI⁺) 491.8 (M+H).

Example 11: Preparation ofN-((4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)-1-piperidinyl)(phenoxy)phosphinyl)-L-alaninemethyl ester (Compound 12)

Phenyl phosphorodichloridate (4.0 g, 18.96 mmol, 1.0 eq.), L-alaninemethyl ester hydrochloride (2.64 g, 18.96 mmol, 1.0 eq.) were dissolvedin DCM (40 mL). To the mixture at −78 to −70° C., Et₃N (3.83 g, 37.92mmol, 2.0 eq.) was added dropwise. The mixture was stirred for 1 h undernitrogen, and then concentrated under reduced pressure. The residualmaterial was purified by flash column chromatography (silica-gel;eluent: PE:EA, 3:1), giving N-(chloro(phenoxy)phosphinyl)-L-alaninemethyl ester (2.0 g, 38.1%): ¹H NMR (CDCl₃, 500 MHz) δ ppm 1.52-1.57 (m,3H), 3.78-3.85 (m, 3H), 4.16-4.26 (m, 2H), 7.30 (d, J=10 Hz, 3H),7.36-7.44 (m, 2H).4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (208 mg, 0.5 mmol, 1.0 eq.) and(chloro(phenoxy)phosphinyl)-L-alanine methyl ester (140 mg, 0.5 mmol,1.0 eq.) were dissolved in DCM (5 mL), followed by addition of Et₃N (101mg, 1.0 mmol, 2.0 eq.). The mixture was stirred for 12 h under nitrogen,and then concentrated under reduced pressure. The residual material waspurified by flash column chromatography (silica-gel; eluent: PE:EA,2:1), giving compound 12 (120 mg, 38.5%): ¹H NMR (CD₃OD, 500 MHz) δ ppm1.39 (dd, J=15 Hz, 10 Hz, 3H), 1.52-1.57 (m, 2H), 1.86-1.90 (m, 2H),2.82-2.89 (m, 2H), 3.72 (d, J=10 Hz, 6H), 3.93-3.96 (m, 2H), 4.64 (s,1H), 7.15-7.22 (m, 3H), 7.34-7.37 (m, 2H), 7.45-7.51 (m, 3H), 8.35 (s,1H); m/z (ESI⁺) 622.9 (M+H).

Example 12: Preparation of4-(2,6-dichlorobenzamido)-N-(1-(2-oxido-4H-benzo[d][1,3,2]dioxaphosphinin-2-yl)piperidin-4-yl)-1H-pyrazole-3-carboxamide(Compound 13)

2-(Hydroxymethyl)phenol (2.0 g, 16.1 mmol, 1.0 eq.) and POCl₃ (2.7 g,17.7 mmol, 1.1 eq.) were dissolved in THF (40 mL), followed by additionof Et₃N (3.4 g, 35.8 mmol, 2.1 eq.) dropwise while the system was cooledto −78 and −70° C. The mixture was stirred for 1 h under nitrogen andthen concentrated under reduced pressure. The residual material waspurified by flash column chromatography (silica-gel; eluent: PE:EA, 3:1)to afford 2-chloro-2-oxo-4H-1,3,2-benzodioxaphosphinine (2.3 g, 70.0%):¹H NMR (CDCl₃, 500 MHz): δ ppm 5.51-5.57 (m, 2H), 7.13-3.16 (m, 2H),7.25-7.29 (m, 1H), 7.39-7.43 (m, 1H).4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) and2-chloro-2-oxo-4H-1,3,2-benzodioxaphosphinine (204 mg, 1.0 mmol, 1.0eq.) were dissolved in DCM (10 mL), followed by addition of Et₃N (202mg, 2.0 mmol, 2.0 eq.). The mixture was stirred for 12 h under nitrogen.The mixture was concentrated under reduced pressure, and the residualmaterial was purified by flash column chromatography (silica-gel;eluent: PE:EA, 1:1), giving compound 13 (300 mg, 54.5%): ¹H NMR (CD₃OD,500 MHz) δ ppm 1.59-1.64 (m, 2H), 1.92 (d, J=10 Hz, 2H), 2.98 (t, J=15Hz, 2H), 3.58 (s, 2H), 4.0-4.03 (m, 1H), 5.28-5.35 (m, 1H), 5.51-5.53(m, 1H), 7.11-7.12 (m, 1H), 7.19 (d, J=10 Hz, 1H), 7.26 (d, J=10 Hz,1H), 7.38 (s, 1H), 7.47-7.52 (m, 3H), 8.36 (s, 1H); ¹³C NMR (CD₃OD, 125MHz) δ ppm 32.96, 44.83, 47.44, 68.53, 119.20, 122.59, 123.01, 123.26,125.30, 126.97, 129.48, 130.96, 132.78, 133.45, 134.42, 136.68, 152.47,163.29, 164.66; m/z (ESI⁺) 549.8 (M+H).

Example 13: Synthesis ofN-((4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidin-1-yl)(naphthalen-1-yloxy)phosphinyl)-L-alaninemethyl ester (Compound 16)

1-Naphthol (0.72 g, 4.99 mmol, 1.0 eq.) and phosphorus oxychloride (767mg, 4.99 mmol, 1.0 eq.) were suspended in anhydrous ether (20 mL), andthe temperature was cooled to −78° C. Triethylamine (505 mg, 4.99 mmol,1.0 eq.) was added dropwise to the mixture, and the reaction mixture wasstirred at −78° C. for 0.5 h. The reaction mixture was warmed up to r.t.and stirred at r.t. overnight. The mixture was filtered, and thefiltrate was concentrated to give crude 1-naphthyl phosphorodichloridateas light yellow oil (1.1 g, 85.0%), which was used without purification.To a stirred solution of 1-naphthyl phosphorodichloridate (1.1 g, 4.2mmol, 1.0 eq.) and L-alanine methyl ester hydrochloride (586 mg, 4.2mmol, 1.0 eq.) in anhydrous DCM (30 mL) was added dropwise anhydrous TEA(848 mg, 8.4 mmol, 2.0 eq.) at −78° C. under nitrogen. The reactionmixture was stirred at −78° C. for 1 h and then at room temperature for1 h. The solvent was removed under reduced pressure and the residue waspurified by flash column chromatography (silica-gel; eluting: PE:EA,1:1), giving N-(chloro(1-naphthyloxy)phosphinyl)-L-alanine methyl ester(790 mg, 57.4%). To a stirred solution of the4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (410 mg, 0.98 mmol, 1.1 eq.) and TEA (198 mg, 1.96 mmol,2.2 eq.) in anhydrous DCM (10 mL) was added dropwise, at 0° C. undernitrogen, N-(chloro(1-naphthyloxy)phosphinyl)-L-alanine methyl ester(289 mg, 0.88 mmol, 1.0 eq.). The reaction mixture was stirred at roomtemperature for 5 h. The solvent was removed under reduced pressure andthe residue was purified by flash column chromatography (silica-gel;eluent: DCM:MeOH, 20:1), affording compound 16 (226 mg, 38.1%): ¹H NMR(500 MHz, CD₃OD) δ ppm 1.59-1.32 (m, 5H), 1.81 (s, 2H), 2.81 (d, J=23.5Hz, 2H), 3.81-3.64 (m, 5H), 3.87 (s, 1H), 4.00 (s, 1H), 7.59-7.32 (m,7H), 7.66 (s, 1H), 7.86 (d, J=6.8 Hz, 1H), 8.17 (dd, J=15.0, 7.9 Hz,1H), 8.31 (s, 1H); ¹³C NMR (125 MHz, CD₃OD) δ ppm 20.68, 33.01, 45.18,47.65, 51.02, 52.71, 115.90, 122.32, 122.63, 122.72, 122.96, 125.39,125.49, 126.56, 127.31, 127.68, 128.87, 129.43, 132.73, 133.40, 134.49,136.27, 136.62, 148.32, 163.20, 164.62, 175.83; m/z (ESI⁻) 670.7 (M−H).

Example 14: Preparation ofN-((4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidin-1-yl)(naphthalen-1-yloxy)phosphinyl)-L-alanineisopropyl ester (Compound 17)

4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) andN-(chloro(1-naphthyloxy)phosphinyl)-L-alanine isopropyl ester (356 mg,1.0 mmol, 1.0 eq.) were dissolved in DCM (15 mL), followed by additionof Et₃N (303 mg, 3.0 mmol, 2.0 eq.). The mixture was stirred for 12 hunder nitrogen, and then concentrated under reduced pressure. Theresidual material was purified by flash column chromatography(silica-gel; eluent: DCM:MeOH, 30:1), affording compound 17 (200 mg,29%): ¹H NMR (CD₃OD, 500 MHz) δ ppm 1.21-1.37 (m, 6H), 1.40-1.44 (m,4H), 1.53 (t, J=10 Hz, 1H), 1.85 (s, 2H), 2.86 (s, 2H), 3.78 (s, 2H),3.88-4.0 (m, 2H), 4.99-5.03 (m, 1H), 7.43-7.57 (m, 7H), 7.70 (s, 1H),7.88 (s, 1H), 8.18-8.33 (m, 1H), 8.33 (s, 1H); ³¹P NMR (CD₃OD, 203 MHz):δ ppm 10.83, 11.40; m/z (ESI⁺) 701.1 (M+H).

Example 15: Preparation of isopropyl((4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidin-1-yl)(phenoxy)phosphoryl)-L-alaninate(Compound 18)

Phenyl phosphorodichloridate (2.0 g, 9.5 mmol, 1.0 eq.) and L-alanineisopropyl ester hydrochloride (1.6 g, 9.5 mmol, 1.0 eq.) were dissolvedin DCM (20 mL). To the mixture was added Et₃N (1.9 g, 19 mmol, 2.0 eq.)dropwise at −78 to −70° C. The mixture was stirred for 1 h undernitrogen, and concentrated under reduced pressure. The residual materialwas purified by flash column chromatography (silica-gel; eluent: PE:EA,3:1), affording N-(chloro(phenoxy)phosphinyl)-L-alanine isopropyl ester(1.9 g, 65.4%).4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (417 mg, 1.0 mmol, 1.0 eq.) andN-(chloro(phenoxy)phosphinyl)-L-alanine isopropyl ester (305 mg, 1.0mmol, 1.0 eq.) were dissolved in DCM (10 mL), followed by addition ofEt₃N (202 mg, 2.0 mmol, 2.0 eq.). The mixture was stirred for 12 h undernitrogen, and then concentrated under reduced pressure. The residualmaterial was purified by flash column chromatography (silica-gel;eluent: PE:EA, 2:1), giving compound 18 (200 mg, 30.7%): ¹H NMR (CD₃OD,500 MHz) δ ppm 1.27-1.31 (m, 6H), 1.38-1.44 (m, 3H), 1.56 (d, J=15 Hz,2H), 1.93 (s, 2H), 2.87 (s, 2H), 3.77 (s, 2H), 3.94-3.97 (m, 2H),5.03-5.06 (m, 1H), 7.25-7.26 (m, 3H), 7.38-7.40 (m, 2H), 7.50-7.56 (m,3H), 8.39 (s, 1H); ¹³C NMR (CD₃OD, 125 MHz) δ ppm 20.52, 21.82, 32.88,44.84, 47.67, 51.06, 69.90, 121.31, 121.47, 122.41, 122.82, 125.53,129.32, 130.52, 132.62, 133.30, 134.24, 136.52, 152.38, 163.12, 164.48,174.72; m/z (ESI⁺) 651.0 (M+H).

Example 16: Preparation of4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-methanephosphonicacid disodium salt (Compound 20)

4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (1.04 g, 2.5 mmol, 1.0 eq.) and (diethoxyphosphoryl)methyl4-methylbenzenesulfonate (0.81 g, 2.5 mmol, 1.0 eq.) were dissolved inDMF (10 mL), followed by addition of Et₃N (732 mg, 7.15 mmol, 3.0 eq.).The mixture was stirred for 12 h, and then concentrated under reducedpressure. The residual material was purified by flash columnchromatography (silica-gel; eluent: DCM:MeOH, 10:1), giving4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-methanephosphonicacid diethyl ester (320 mg, 24%).4-(4-(2,6-Dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-methanephosphonicacid diethyl ester (300 mg, 0.56 mmol, 1.0 eq.) was dissolved in CH₃CN(5 mL), followed by addition of TMSBr (260 mg, 1.7 mmol, 3.0 eq.). Themixture was stirred for 36 h under nitrogen, diluted with MeOH (10 mL).The solid material was collected by filtration, and the filter cake waswashed with MeOH (10 mL) and dried, affording4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-methanephosphonicacid (100 mg, 38%). This phosphonic acid (100 mg, 0.21 mmol, 1.0 eq.)was dissolved in H₂O (5 mL), and treated with NaOH (16.8 mg, 0.42 mmol,2.0 eq.). The mixture was stirred for 0.5 h and then lyophilized, givingcompound 20 (100 mg, 92%): ¹H NMR (CD₃OD, 500 MHz) δ ppm 1.31 (d, J=15Hz, 1H), 1.67-1.75 (m, 2H), 1.90-1.93 (m, 2H), 2.39 (t, J=10 Hz, 2H),2.58 (d, J=10 Hz, 2H), 3.27 (s, 1H), 3.84 (s, 1H), 7.41-7.49 (m, 3H),8.26 (s, 1H); ¹³C NMR (CD₃OD, 125 MHz) δ ppm 32.29, 47.10, 55.32, 58.60,59.72, 123.31, 124.30, 129.44, 132.59, 133.51, 134.16, 137.02, 163.30,164.94; ³¹P NMR (CD₃OD, 203 MHz) δ ppm 13.86; m/z (ESI⁺) 477.6 (M+H).

Example 17: Preparation of(4-(2,6-dichlorobenzamido)-3-(piperidin-4-ylcarbamoyl)-1H-pyrazol-1-yl)methylisopropyl carbonate hydrochloride (Compound 25)

Compound A (481 mg, 1.0 mmol, 1.0 eq.) and chloromethyl isopropylcarbonate (304 mg, 2.0 mmol, 2.0 eq.) were dissolved in CH₃CN (10 mL),followed by addition of NaHCO₃ (168 mg, 2.0 mmol, 2.0 eq.). The mixturewas stirred for 12 h under nitrogen at 25° C. and then concentratedunder reduced pressure. The residual material was purified by flashcolumn chromatography (silica-gel; eluent: PE:EA, 1:1), affordingtert-butyl4-(4-(2,6-dichlorobenzamido)-1-((isopropoxycarbonyloxy)methyl)-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(240 mg, 40.1%). The product thus obtained (240 mg, 0.4 mmol, 1.0 eq.)was dissolved in 1,4-dioxane (4 mL), followed by addition of 4M HCl in1,4-dioxane (2 mL). The mixture was stirred for 12 h, and thenconcentrated under reduced pressure. The residual material was purifiedby flash column chromatography (silica-gel; eluent: DCM:MeOH, 20:1),affording compound 25 (100 mg, 46.7%): ¹H NMR (D₂O, 500 MHz) δ ppm1.26-1.28 (m, 6H), 1.79-1.87 (m, 2H), 2.17 (d, J=15 Hz, 2H), 3.14 (t,J=10 Hz, 2H), 3.50 (d, J=10 Hz, 2H), 4.03 (s, 1H), 4.89-4.94 (m, 1H),6.13 (s, 2H), 7.41 (s, 3H), 8.53 (s, 1H); ¹³C NMR (D₂O, 125 MHz) δ ppm20.72, 20.81, 27.72, 42.87, 44.02, 75.07, 120.84, 125.87, 128.25,131.44, 132.08, 133.65, 136.14, 153.91, 162.50, 164.59; m/z (ESI⁺) 497.8(M+H).

Example 18: Preparation of4-(2,6-dichlorobenzamido)-1-dodecanoyl-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamide(Compound 27)

4-(2,6-Dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (1.6 g, 3.8 mmol, 1.0 eq.) and (9H-fluoren-9-yl)methylcarbonochloridate (1.0 g, 3.8 mmol, 1.0 eq.) were dissolved indioxane-H₂O (20 mL, 1:1), followed by addition of NaHCO₃ (640 mg, 7.6mmol, 2.0 eq.). The mixture was stirred for 12 h, and then concentratedunder reduced pressure. The residual material was purified by flashcolumn chromatography (silica-gel; eluent: PE:EA, 1:1), affording(9H-fluoren-9-yl)methyl4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(1.0 g, 43.6%). (9H-fluoren-9-yl)methyl4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(900 mg, 1.5 mmol, 1.0 eq.) and dodecanoyl chloride (358 mg, 1.64 mmol,1.1 eq.) were dissolved in DCM (10 mL), followed by addition of Et₃N(303 mg, 3.0 mmol, 2.0 eq.). The mixture was stirred for 12 h undernitrogen, and then concentrated under reduced pressure. The residualmaterial was purified by flash column chromatography (silica-gel;eluent: PE:EA, 5:1), giving (9H-fluoren-9-yl)methyl4-(4-(2,6-dichlorobenzamido)-1-dodecanoyl-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(800 mg, 68%). (9H-Fluoren-9-yl)methyl4-(4-(2,6-dichlorobenzamido)-1-dodecanoyl-1H-pyrazole-3-carboxamido)piperidine-1-carboxylate(560 mg, 0.71 mmol, 1.0 eq.) was dissolved in DMF (5 mL), and treatedwith DIPEA (5 mL). The mixture was stirred for 48 h, and thenconcentrated under reduced pressure. The residual material was purifiedby flash column chromatography (silica-gel; eluent: PE:EA, 2:1),affording compound 27 (150 mg, 68%): ¹H NMR (CD₃OD, 500 MHz) δ ppm0.89-1.01 (m, 3H), 1.30 (s, 17H), 1.50-1.61 (m, 3H), 1.96 (d, J=10 Hz,2H), 2.40 (s, 2H), 2.80 (t, J=15 Hz, 1H), 3.21 (t, J=15 Hz, 1H), 3.98(t, J=15 Hz, 1H), 4.10 (s, 1H), 4.50 (d, J=10 Hz, 1H), 7.46-7.51 (m,3H), 8.36 (s, 1H); ¹³C NMR (CD₃OD, 125 MHz) δ ppm 14.38, 23.67, 26.64,30.40, 30.44, 30.48, 30.58, 30.68, 32.39, 33.02, 33.28, 34.12, 41.87,45.87, 47.63, 122.35, 123.02, 129.48, 132.76, 133.47, 134.53, 136.69,163.26, 164.81, 174.11; m/z (ESI⁺) 564.0 (M+H).

Example 19: Preparation of((4-(4-(2,6-dichlorobenzamido)-1-dodecanoyl-1H-pyrazole-3-carboxamido)piperidin-1-yl)(phenoxy)phosphinyl)-L-alaninemethyl ester (Compound 38)

Compound 12 (310 mg, 0.5 mmol, 1.0 eq.) and dodecanoyl chloride (130 mg,0.6 mmol, 1.2 eq.) were dissolved in DCM (5 mL), followed by addition ofEt₃N (101 mg, 1.0 mmol, 2.0 eq.). The mixture was stirred for 12 h undernitrogen, and then concentrated under reduced pressure. The residualmaterial was purified by flash column chromatography (silica-gel;eluent: PE:EA, 3:1), affording compound 38 (120 mg, 30%): ¹H NMR (CD₃OD,500 MHz) δ ppm 0.92 (s, 3H), 1.32-1.45 (m, 21H), 1.61 (s, 2H), 1.78-1.90(m, 4H), 2.84 (s, 2H), 3.23 (s, 2H), 3.73 (s, 4H), 3.96 (s, 1H),7.18-7.24 (m, 3H), 7.37 (s, 2H), 7.50 (s, 3H), 8.93 (s, 1H); ¹³C NMR(CD₃OD, 125 MHz) δ ppm 14.46, 20.68, 23.68, 25.19, 30.08, 30.41, 30.56,30.67, 32.85, 33.00, 34.12, 45.00, 45.21, 48.22, 50.98, 52.72, 120.46,121.41, 121.57, 125.23, 125.67, 129.49, 130.64, 132.91, 133.30, 136.21,138.79, 152.46, 163.30, 163.46; ³¹P NMR (CD₃OD, 203 MHz) δ ppm 10.54,11.09; m/z (ESI⁺) 805.2 (M+H).

Example 20: Synthesis of4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-aceticacid hydrobromide (Compound 54)

To a stirred solution of4-(2,6-dichlorobenzamido)-N-(piperidin-4-yl)-1H-pyrazole-3-carboxamidehydrochloride (900 mg, 2.1 mmol, 1.0 eq.) and Triethylamine (530 mg, 5.3mmol, 2.5 eq.) in DCM (25 mL) was added, dropwise under nitrogen,tert-butyl 2-bromoacetate (419 mg, 2.1 mmol, 1.0 eq.). The reactionmixture was stirred overnight at room temperature. The solvent wasremoved under reduced pressure and the residue was purified by flashcolumn chromatography (silica-gel; eluent: DCM:MeOH, 20:1), affordingtert-butyl4-(4-(2,6-dichlorobenzamido)-1H-pyrazole-3-carboxamido)piperidine-1-acetate(620 mg, 59.5%): ¹H NMR (500 MHz, CD₃OD) δ ppm 1.46 (s, 9H), 1.70 (d,J=10.9 Hz, 2H), 1.89 (d, J=11.7 Hz, 2H), 2.30 (t, J=11.5 Hz, 2H), 2.94(d, J=10.4 Hz, 2H), 3.13 (s, 2H), 3.84 (s, 1H), 7.47 (dd, J=16.4, 6.6Hz, 3H), 8.33 (s, 1H). To a stirred solution of this acetate derivative(620 mg, 1.2 mmol, 1.0 eq.) in anhydrous DCM (16 mL) was added TFA (8mL). The reaction mixture was stirred overnight at room temperature.Solvent was removed under reduced pressure and the residue was treatedwith 40% HBr (5 mL) and lyophilized, giving compound 54 (533 mg, 85.2%):¹H NMR (500 MHz, D₂O) δ ppm 2.04 (d, J=13.2 Hz, 2H), 2.32 (d, J=13.4 Hz,2H), 3.30 (t, J=12.3 Hz, 2H), 3.82 (d, J=11.9 Hz, 2H), 4.13 (d, J=28.8Hz, 3H), 7.54 (d, J=6.5 Hz, 1H), 7.56 (s, 2H), 8.40 (s, 1H); ¹³C NMR(125 MHz, DMSO-d₆) δ ppm 28.42, 43.94, 51.85, 55.33, 121.65, 128.55,131.35, 132.06, 132.39, 135.42, 160.59, 162.85, 167.21; m/z (ESI⁺) 439.8(M+H).

Example 21: Toxicity Study in Mice

Male mice (BABL/c) of 20 to 22 g were maintained under standardconditions and randomized into groups. On day 1, three groups of animalswere administered intravenously AT7519 (methanesulfonate salt form),compound 11, and compound 12, respectively. Doses were calculated andexpressed in mmol/kg-body weight, and drug tolerability,pharmacokinetics, and body weight effect were assessed.

(a) Tolerability: Sixty animals were divided into 3 groups (20 eachgroup), and dosed with each test compound: AT7519, 0.031 mmol/kg (anequivalent to 12 mg/kg of AT7519 free form); compound 11, 0.062 mmol/kg;compound 12, 0.124 mmol/kg, respectively. Another group of animals (5 inthe group) were given AT7519 at a dose of 0.039 mmol/kg (15 mg/kg) asreference. The results are summarized in Table 2.

TABLE 2 Animal death after i.v.-administration of different compoundsCompound AT7519 Compound 11 Compound 12 Dose (mmol/kg) 0.031 0.039 0.0620.124 Animals in group 20 5 20 20 Number of deaths 4 5 0 0 Death rate(%) 20 100 0 0

As indicated by the data in Table 2, the low dose (0.031 mmol/kg) ofAT7519 caused animal death rate of 20%, while the high dose (0.039mmol/kg) of AT7519 killed all the animals in the group even though thedose was only increased by 25% (from the low dose), indicating that0.031 mmol/kg was a threshold lethal dose of AT7519. In contrast,compounds 11 and 12 did not cause a single death even if the compoundswere dosed at a level of 2-fold and 4-fold of molar-equivalents to theAT7519 threshold level. In summary, compounds 11 and 12 were much lesstoxic than AT7519.

(b) Toxicokinetics: In order to confirm the validity of the abovetox-study, plasma AT7519 concentration after administration of eachcompound was determined. The i.v. doses of AT7519, compound 11, andcompound 12 were the same as above, namely 0.031 mmol/kg, 0.062 mmol/kg,and 0.124 mmol/kg, respectively. Blood samples were collected at 2 min,10 min, 1 h, and 4 h. Concentration of T7519 was analyzed in each sampleusing LC-MS/MS method. The results are summarized in Table 3, and theconcentration-time curves are illustrated in FIG. 1.

TABLE 3 Concentration* of AT7519 in plasma of mice from toxicokineticsstudy Compound AT7519 Compound 11 Compound 12 Dose (mmol/kg) 0.031 0.0620.124 Dosing route I.V . I.V . I.V . Dosing Conc. (mM) 0.0031 0.00620.0124 Dosing volume (mL/kg) 10 10 10 2 min 10230 45000 99067 10 min1837 12627 17867 1 h 489 970 1657 4 h 47 170 197 *The concentration isin ng/mL.

The data in Table 3 show that both compounds 11 and 12 were converted toAT7519 within a very short time (<2 min) after intravenous injection.For each time point, there was a rough correlation between the plasmaconcentration and the dose, regardless of whether the compoundadministered was AT7519 itself or its prodrugs (Compound 11, or Compound12). In the cases of Compounds 11 and 12, the plasma AT7519 exposureswere much higher.

(c) Drug effect on animal body weight after a single dose intravenously:Sixty animals were divided into 3 groups (20 in each group), and on day0 (the initial day of the study) dosed with each test compound: AT7519,0.031 mmol/kg (an equivalent to 12 mg/kg of AT7519 free form); compound11, 0.062 mmol/kg; or compound 12, 0.124 mmol/kg, respectively. Clinicalobservations were made in the following schedule: continuous observationin the first four hours after dosing, and then twice daily, at one weektime, and at day 14. The parameters for observation included animal'sphysical and mental behaviors, autonomous activity, hair, glandsecretion, feces, and death. Body temperature was taken at pre-dosing,and on days 3, 5, 7, and 10 post-dosing.

In the study, 4 animals died in the AT7519 group, and no animal deathwas observed in groups dosed with compounds 11 and 12.

The body weights of the animals are summarized in Table 4, and the trendlines for animal body weight changes in each group are given in FIG. 2.The body weight was average weight of all the animals in the group froma single measurement.

TABLE 4 Animal body-weight changes after dosing Body weight (g) CompoundDay 0 Day 1 Day 2 Day 4 Day 7 Day 10 AT7519 19.44 19.53 19.45 20.9420.83 20.63 11 19.16 18.58 18.83 19.95 20.16 20.52 12 19.75 18.70 19.1719.95 20.79 21.30

The results indicated that during the first few days, the body weightsfor animals receiving high doses of compounds (compounds 11 and 12) hada trend of decrease but within a narrow range, i.e., 3 to 5% incomparison to that receiving AT7519. On day 7 and afterwards, bodyweights of animals were the same or very similar across all groups. Itwas postulated that the initial body weight decrease was due to thenormal reaction of the animals to a very high dose of compounds given tothe animals.

Example 22: Toxicokinetic Study in Rats

Male SD (Sprague Dawley) rats of body weight 220 to 240 g weremaintained under standard conditions and randomized into three groups.On day 0 (initial day), all the animals were given one of the threecompounds intravenously. Dose was calculated in mmol/kg.

(a) Dose exploration: One animal from each group was given the presethigh dose of each compound. Observations are given in Table 5.

TABLE 5 Toxicity of the test compounds Body Animal weight Dose CompoundNo. (g) (mmol/kg) Animal death AT7519 1 244 0.049 Died immediatelypost-dosing 11 7 233 0.055 Died at 2 min post-dosing 12 13 237 0.125Behaved normally

The data in Table 5 showed that only compound 12 did not induce theanimal death while both AT7519 and compound 11 were already at theirlethal doses (doses are shown in the table).

(b) TK study: The remaining animals were randomized into three groups,with 6 in each group. At time 0, animals were administered either AT7519(dose, 0.039 mmol/kg), or compound 11 (0.050 mmol/kg), or compound 12(0.124 mmol/kg). TK analysis was conducted as follows: Blood sampleswere collected at time points of 2 min, 10 min, 1 h, 2 h, and 6 h intosample tube (heparinized). After converting to plasma samples, AT7519concentration was analyzed (LC-MS/MS). The results are summarized inTable 6, and the concentration-time curves are given in FIG. 3.

TABLE 6 Plasma AT7519 concentration in rat TK study Compound AT7519 1112 Dose (mmol/kg) 0.039 0.050 0.124 Dosing route I.V . I.V . I.V .Solution Conc. (mM) 0.0039 0.0050 0.0125 Dosing Volume (mL/kg) 10 10 10Time AT7519 concentration (ng/mL) 2 min 19125 27680 117000 10 min 46005896 34400 1 h 814 891 2798 4 h 554 601 1530 6 h 148 159 449

Example 23: Toxicity Study in Rats

Male SD (Sprague Dawley) rats were dosed intravenously with 0.031mmol-equivalent/kg of each test compound, with the injection timecontrolled between 30 to 45 seconds. A four-level score system wasapplied to describe the toxicity of the test compound: A, animal diedduring the injection; B, animal experienced shock within 5 minutes afterintravenous administration, and falling to the ground and decreasingactivity after recovery; C, no animal death but falling to the groundwithin 30 min with decreasing activity; D, no animal death, no obviousabnormal behavior, and no obvious body-weight decrease. For the resultsfrom selected compounds, see Table 7.

TABLE 7 Toxicity scores in rats Compound Toxicity Score AT7519 B 2 C 3 D4 D 5 C 6 C 7 D 8 C 10 C 11 D 12 D 13 C 16 D 17 B 18 D 20 B 25 A 27 C 38D 54 D

Although this invention is described in detail with reference toembodiments thereof, these embodiments are offered to illustrate but notto limit the invention. It is possible to make other embodiments thatemploy the principles of the invention and that fall within its spiritand scope as defined by the claims appended hereto.

The contents of all documents and references cited herein are herebyincorporated by reference in their entirety.

What is claimed is: 1.-28. (canceled)
 29. A compound which is:

or a pharmaceutically acceptable salt or ester thereof.
 30. The compoundof claim 29, wherein the compound is:


31. A pharmaceutical composition comprising the compound of claim 29 anda pharmaceutically acceptable carrier.
 32. The pharmaceuticalcomposition of claim 31, wherein the composition is suitable for oraladministration.
 33. The pharmaceutical composition of claim 32, whereinthe composition is in the form of a hard shell gelatin capsule, a softshell gelatin capsule, a cachet, a pill, a tablet, a lozenge, a powder,a granule, a pellet, a solution, a pastille, a dragee, an emulsion, anelixir, or a syrup.
 34. The pharmaceutical composition of claim 31,wherein the composition is injectable.
 35. The pharmaceuticalcomposition of claim 34, wherein the composition is suitable forintravenous, intramuscular, intraperitoneal, or subcutaneousadministration.
 36. A method for the inhibition or modulation of acyclin dependent kinase (CDK) and/or glycogen synthase kinase-3 (GSK-3)in a subject, comprising administering to the subject an effectiveamount of the compound of claim 29, such that the CDK and/or GSK-3 isinhibited or modulated in the subject.
 37. The method of claim 36,wherein the subject suffers from a disease state or condition mediatedby CDK and/or GSK-3.
 38. The method of claim 37, wherein the diseasestate or condition is a tumor or a cancer.
 39. A method for treating adisease state or condition mediated by a cyclin dependent kinase (CDK)and/or glycogen synthase kinase-3 (GSK-3) in a subject, comprisingadministering to the subject an effective amount of the compound ofclaim 29 or a pharmaceutically acceptable salt or ester thereof, suchthat the disease state or condition is treated in the subject.
 40. Themethod of claim 39, wherein CDK and/or GSK-3 is inhibited or modulatedin the subject.
 41. The method of claim 39, wherein the disease state orcondition is a tumor or a cancer.
 42. A method for treating a tumor or acancer in a subject, comprising administering to the subject aneffective amount of the compound of claim 29 or a pharmaceuticallyacceptable salt or ester thereof, such that the tumor or the cancer istreated in the subject.
 43. The method of claim 42, wherein the tumor orcancer is selected from multiple myeloma (MM), chronic lymphocyticleukemia (CLL), acute myeloid leukema (AML), mantle cell lymphoma (MCL),solid tumors, refractory solid tumors, non-Hodgkin lymphoma,hematological neoplasm, neuroblastoma, colorectal cancer, cervicalcancer, lung cancer, leukemia, breast cancer, pancreatic cancer, B-cellmalignancy, neoplasm, metastatic tumor, carcinoma of the colon, andmyelodysplastic syndrome.
 44. The method of claim 42, wherein theeffective amount is an amount effective to inhibit abnormal cell growth.45. The method of claim 42, wherein the subject is a mammal.
 46. Themethod of claim 46, wherein the mammal is a human.
 47. The method ofclaim 42, wherein said administering comprises intravenous,intramuscular, intraperitoneal, or subcutaneous administration.
 48. Themethod of claim 42, wherein said administering comprises oraladministration.